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BEGIN:VEVENT
DTSTART;VALUE=DATE:20260101
DTEND;VALUE=DATE:20260501
DTSTAMP:20260405T221824
CREATED:20250904T185549Z
LAST-MODIFIED:20250904T185549Z
UID:10000122-1767225600-1777593599@acrpnet.org
SUMMARY:Spring 2026 Initial Certification Regular Registration
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/spring-2026-initial-certification-regular-registration
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260215
DTEND;VALUE=DATE:20260416
DTSTAMP:20260405T221824
CREATED:20250904T191217Z
LAST-MODIFIED:20251125T165425Z
UID:10000126-1771113600-1776297599@acrpnet.org
SUMMARY:Spring 2026 Certification Maintenance Early Bird Registration
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/spring-2026-certification-maintenance-early-bird-registration
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260215
DTEND;VALUE=DATE:20260516
DTSTAMP:20260405T221824
CREATED:20250904T185839Z
LAST-MODIFIED:20250904T185839Z
UID:10000124-1771113600-1778889599@acrpnet.org
SUMMARY:Spring 2026 Initial Certification Testing Dates
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/spring-2026-initial-certification-testing-dates
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Denver:20260406T170000
DTEND;TZID=America/Denver:20260406T183000
DTSTAMP:20260405T221824
CREATED:20260302T180222Z
LAST-MODIFIED:20260302T180222Z
UID:10000235-1775494800-1775500200@acrpnet.org
SUMMARY:Colorado Chapter: Maintaining Data Integrity from Collection to Reporting and Everything in Between (ACRP 2024 Conference Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/colorado-chapter-maintaining-data-integrity-from-collection-to-reporting-and-everything-in-between-acrp-2024-conference-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260408T120000
DTEND;TZID=America/New_York:20260408T130000
DTSTAMP:20260405T221824
CREATED:20260313T180511Z
LAST-MODIFIED:20260313T180511Z
UID:10000244-1775649600-1775653200@acrpnet.org
SUMMARY:Virginia Chapter: AI in Medicine: Past\, Present\, and Future
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/virginia-chapter-ai-in-medicine-past-present-and-future
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20260408T180000
DTEND;TZID=America/Chicago:20260408T193000
DTSTAMP:20260405T221824
CREATED:20260217T225733Z
LAST-MODIFIED:20260217T225733Z
UID:10000223-1775671200-1775676600@acrpnet.org
SUMMARY:St. Louis Chapter: Assessing and Managing Study Coordinator Workload (ACRP 2025 Conference Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/st-louis-chapter-assessing-and-managing-study-coordinator-workload-acrp-2025-conference-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260408T180000
DTEND;TZID=America/New_York:20260408T193000
DTSTAMP:20260405T221824
CREATED:20260317T184653Z
LAST-MODIFIED:20260317T184653Z
UID:10000246-1775671200-1775676600@acrpnet.org
SUMMARY:New Jersey Chapter: Modernizing Patient Recruitment: AI Tools\, Workflows\, and Outcomes
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/new-jersey-chapter-modernizing-patient-recruitment-ai-tools-workflows-and-outcomes
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20260409T173000
DTEND;TZID=America/Chicago:20260409T193000
DTSTAMP:20260405T221824
CREATED:20260313T190018Z
LAST-MODIFIED:20260326T144502Z
UID:10000245-1775755800-1775763000@acrpnet.org
SUMMARY:Greater San Antonio Chapter: Efficiency Unleashed: Optimizing Clinical Research Onboarding and Education (ACRP Webinar Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/san-antonio-chapter-efficiency-unleashed-optimizing-clinical-research-onboarding-and-education-acrp-webinar-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Denver:20260414T170000
DTEND;TZID=America/Denver:20260414T190000
DTSTAMP:20260405T221824
CREATED:20260327T145848Z
LAST-MODIFIED:20260327T145848Z
UID:10000254-1776186000-1776193200@acrpnet.org
SUMMARY:Greater Salt Lake City Chapter: Spring 2026 Networking Event
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/greater-salt-lake-city-chapter-spring-2026-networking-event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260415T120000
DTEND;TZID=America/New_York:20260415T130000
DTSTAMP:20260405T221824
CREATED:20260211T232459Z
LAST-MODIFIED:20260211T232459Z
UID:10000216-1776254400-1776258000@acrpnet.org
SUMMARY:Building Trust Through Understanding: Health Literacy in Clinical Research
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/building-trust-through-understanding-health-literacy-in-clinical-research
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260416
DTEND;VALUE=DATE:20260601
DTSTAMP:20260405T221824
CREATED:20250904T191104Z
LAST-MODIFIED:20250904T191104Z
UID:10000125-1776297600-1780271999@acrpnet.org
SUMMARY:Spring 2026 Certification Maintenance Regular Registration
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/spring-2026-certification-maintenance-regular-registration
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260416T180000
DTEND;TZID=America/New_York:20260416T200000
DTSTAMP:20260405T221824
CREATED:20260312T205134Z
LAST-MODIFIED:20260312T205134Z
UID:10000243-1776362400-1776369600@acrpnet.org
SUMMARY:New Jersey Chapter: 2026 Spring Social
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/new-jersey-chapter-2026-spring-social
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260420T120000
DTEND;TZID=America/New_York:20260420T130000
DTSTAMP:20260405T221824
CREATED:20260324T203614Z
LAST-MODIFIED:20260326T144531Z
UID:10000253-1776686400-1776690000@acrpnet.org
SUMMARY:Atlanta Area Chapter: Streamlining Excellence - Best Practices for Developing Research Site SOPs (ACRP Webinar Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/atlanta-chapter-streamlining-excellence-best-practices-for-developing-research-site-sops-acrp-webinar-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260422T120000
DTEND;TZID=America/New_York:20260422T130000
DTSTAMP:20260405T221824
CREATED:20260121T173404Z
LAST-MODIFIED:20260121T173404Z
UID:10000205-1776859200-1776862800@acrpnet.org
SUMMARY:Kentucky Chapter: Harnessing AI for Patient-Centered Clinical Trial Recruitment
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/kentucky-chapter-harnessing-ai-for-patient-centered-clinical-trial-recruitment
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260424T000000
DTEND;TZID=America/New_York:20260427T235900
DTSTAMP:20260405T221824
CREATED:20240125T174612Z
LAST-MODIFIED:20251203T175622Z
UID:10000015-1776988800-1777334340@acrpnet.org
SUMMARY:ACRP 2026
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/acrp-2026
LOCATION:Hyatt Regency Orlando\, 9801 International Drive\, Orlando\, FL\, 32819\, United States
ATTACH;FMTTYPE=image/png:https://acrpnet.org/wp-content/uploads/2024/01/ACRP26_Evergreen.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260424T190000
DTEND;TZID=America/New_York:20260424T210000
DTSTAMP:20260405T221824
CREATED:20260312T015351Z
LAST-MODIFIED:20260312T015351Z
UID:10000242-1777057200-1777064400@acrpnet.org
SUMMARY:Virginia Chapter: ACRP 2026 Orlando Networking Event
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/virginia-chapter-acrp-2026-orlando-networking-event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20260428T120000
DTEND;TZID=America/Los_Angeles:20260428T133000
DTSTAMP:20260405T221824
CREATED:20260403T141008Z
LAST-MODIFIED:20260403T141008Z
UID:10000257-1777377600-1777383000@acrpnet.org
SUMMARY:PNW Chapter: Principles to Practice: An Understanding of the ICH E6(R3) Update’s Effect on Good Clinical Practice (ACRP 2025 Conference Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/pnw-chapter-principles-to-practice-an-understanding-of-the-ich-e6r3-updates-effect-on-good-clinical-practice-acrp-2025-conference-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260430T173000
DTEND;TZID=America/New_York:20260430T200000
DTSTAMP:20260405T221824
CREATED:20260330T135432Z
LAST-MODIFIED:20260330T135432Z
UID:10000255-1777570200-1777579200@acrpnet.org
SUMMARY:RTP Chapter: Navigating the Realities of Inclusion in Today’s Workplace
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/rtp-chapter-navigating-the-realities-of-inclusion-in-todays-workplace
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260504T170000
DTEND;TZID=America/New_York:20260504T183000
DTSTAMP:20260405T221824
CREATED:20260302T180344Z
LAST-MODIFIED:20260302T180344Z
UID:10000236-1777914000-1777919400@acrpnet.org
SUMMARY:Colorado Chapter: FDA's Latest Guidance on Informed Consent: Reading Between the Lines (ACRP 2025 Conference Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/colorado-chapter-fdas-latest-guidance-on-informed-consent-reading-between-the-lines-acrp-2025-conference-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260506T180000
DTEND;TZID=America/New_York:20260506T210000
DTSTAMP:20260405T221824
CREATED:20260220T193700Z
LAST-MODIFIED:20260220T193700Z
UID:10000230-1778090400-1778101200@acrpnet.org
SUMMARY:NY Metro Chapter: 2026 Spring Networking Event at Electric Shuffle
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/ny-metro-chapter-2026-spring-networking-event-at-electric-shuffle
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20260513T180000
DTEND;TZID=America/Chicago:20260513T193000
DTSTAMP:20260405T221824
CREATED:20260302T180444Z
LAST-MODIFIED:20260302T180444Z
UID:10000237-1778695200-1778700600@acrpnet.org
SUMMARY:St. Louis Chapter: FDA’s Latest Guidance on Informed Consent: Reading Between the Lines  (ACRP 2025 Conference Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/st-louis-chapter-fdas-latest-guidance-on-informed-consent-reading-between-the-lines-acrp-2025-conference-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20260514T173000
DTEND;TZID=America/Chicago:20260514T193000
DTSTAMP:20260405T221824
CREATED:20260319T215906Z
LAST-MODIFIED:20260323T173046Z
UID:10000249-1778779800-1778787000@acrpnet.org
SUMMARY:Greater San Antonio Chapter: 2026 Clinical Trials Day Social
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/greater-san-antonio-chapter-2026-clinical-trials-day-social
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260514T180000
DTEND;TZID=America/New_York:20260514T210000
DTSTAMP:20260405T221824
CREATED:20260317T184741Z
LAST-MODIFIED:20260317T184741Z
UID:10000247-1778781600-1778792400@acrpnet.org
SUMMARY:New England Chapter: Clinical Research Without Borders
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/new-england-chapter-clinical-research-without-borders
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20260519T120000
DTEND;TZID=America/Los_Angeles:20260519T133000
DTSTAMP:20260405T221824
CREATED:20260403T141055Z
LAST-MODIFIED:20260403T141055Z
UID:10000258-1779192000-1779197400@acrpnet.org
SUMMARY:PNW Chapter: FDA Inspection Readiness: Is Your eSource Fit for Purpose? (ACRP 2025 Conference Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/pnw-chapter-fda-inspection-readiness-is-your-esource-fit-for-purpose-acrp-2025-conference-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20260520T170000
DTEND;TZID=America/Los_Angeles:20260520T193000
DTSTAMP:20260405T221824
CREATED:20260309T154609Z
LAST-MODIFIED:20260309T154609Z
UID:10000240-1779296400-1779305400@acrpnet.org
SUMMARY:Phoenix Chapter: 2026 Clinical Trials Day 2026 Event
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/phoenix-chapter-2026-clinical-trials-day-2026-event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Chicago:20260521T173000
DTEND;TZID=America/Chicago:20260521T193000
DTSTAMP:20260405T221824
CREATED:20260220T193755Z
LAST-MODIFIED:20260220T193755Z
UID:10000231-1779384600-1779391800@acrpnet.org
SUMMARY:Greater Kansas City Chapter: Spring 2026 Social
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/greater-kansas-city-chapter-spring-2026-social
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260521T180000
DTEND;TZID=America/New_York:20260521T200000
DTSTAMP:20260405T221824
CREATED:20260224T184445Z
LAST-MODIFIED:20260224T184445Z
UID:10000233-1779386400-1779393600@acrpnet.org
SUMMARY:RTP Chapter: From Framework to Findings - Improving Multicultural Engagement in Clinical Research Through Federally Qualified Health Centers and Community Health Worker Partnerships
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/rtp-chapter-from-framework-to-findings-improving-multicultural-engagement-in-clinical-research-through-federally-qualified-health-centers-and-community-health-worker-partnerships-2
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20260527T120000
DTEND;TZID=America/New_York:20260527T130000
DTSTAMP:20260405T221824
CREATED:20260211T232548Z
LAST-MODIFIED:20260211T232548Z
UID:10000217-1779883200-1779886800@acrpnet.org
SUMMARY:Applied Ethics in Today’s Clinical Research Landscape
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/applied-ethics-in-todays-clinical-research-landscape
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Denver:20260601T170000
DTEND;TZID=America/Denver:20260601T183000
DTSTAMP:20260405T221824
CREATED:20260320T155038Z
LAST-MODIFIED:20260320T155038Z
UID:10000250-1780333200-1780338600@acrpnet.org
SUMMARY:Colorado Chapter: A Holistic CRA Evaluation Process for Improving Monitoring Visits (ACRP 2024 Conference Replay)
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/colorado-chapter-a-holistic-cra-evaluation-process-for-improving-monitoring-visits-acrp-2024-conference-replay
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Denver:20260604T163000
DTEND;TZID=America/Denver:20260604T173000
DTSTAMP:20260405T221824
CREATED:20260401T155356Z
LAST-MODIFIED:20260401T155356Z
UID:10000256-1780590600-1780594200@acrpnet.org
SUMMARY:Greater Salt Lake City Chapter: How AI is Revolutionizing Clinical Trial Patient Recruitment
DESCRIPTION:Standard operating procedures (SOPs) are the backbone of a well-functioning research site\, ensuring compliance\, consistency\, and efficiency in clinical research operations.\nThis webinar provides a comprehensive guide to developing\, implementing\, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes\, enhance regulatory compliance\, and foster team collaboration. Whether you’re starting from scratch or refining existing SOPs\, this session is designed to equip you with actionable insights and tools for success. \nUpon completion of this continuing education program\, participants should be able to: \n\nUnderstand the critical components of research site SOPs and their role in regulatory compliance and operational efficiency.\nIdentify best practices for drafting\, reviewing\, and implementing SOPs that align with industry standards and site-specific needs.\nLearn strategies for ensuring staff adherence to SOPs through effective training and ongoing evaluations.\nExplore methods for regular SOP updates to reflect evolving regulations\, technologies\, and site workflows.\nGain insights into common pitfalls and solutions in SOP development and maintenance.\n\nSpeaker: \n\nSuzanne Rose\, MS\, PhD\, CCRC\, FACRP\, Executive Director of Research\, Stamford Hospital\n\n\nApproved for 1.0 ACRP Contact Hours | Expires June 11\, 2028 \n\n\n	Enrollment OptionsIndividual Enrollment\n\n\nACRP Members without Contact Hours – $0 – Enroll >\n\n\nACRP Members with 1.0 ACRP Contact Hours – $15 – Enroll >\n\n\nNonmembers with 1.0 ACRP Contact Hours – $75 – Enroll >\n\n\nIf you have already enrolled in this course\, or are an ACRP Organization or ACCESS Member through your employer\, please visit your ACRP Learning Portal to access this content.\nNot an ACRP Member? Join Today >\nTeam Enrollment \nEvery step of the way\, ACRP helps organizations efficiently and confidently ensure their study teams are well trained\, prepared\, and supported. Contact us to learn how to bring this program and others to your team.\nLearn More >
URL:https://acrpnet.org/event/greater-salt-lake-city-chapter-how-ai-is-revolutionizing-clinical-trial-patient-recruitment
END:VEVENT
END:VCALENDAR