When in need of a comprehensive refresher, this on-demand eLearning course provides a consolidated overview on the history and importance of ethical conduct in clinical trials involving human subjects.
Learn the various responsibilities of clinical investigators based on FDA Regulations, ICH Guidance Documents, and international standards.
Contact Hours: This course is approved for 7.0 CME hours. No ACRP contact hours are offered. NOTE: This course is not available for individual registration. Upcoming CoursesThis course is available for organizations only. If you are interested in this course for your organization, Contact Us >> Course Description This one-day course will look at the practical application […]
Empower your new coordinators/CRCs to hit the ground running! This intensive 5-day, in-person training for organizations rapidly delivers competent CRCs: positioning your new hires to make an immediate impact — and saving your organization time and money.
Clinical Researcher—June 2018 (Volume 32, Issue 6) PEER REVIEWED Jennifer J. Byrne; Jane M. Shen, PharmD; Amanda W. Wright [DOI: 10.14524/CR-18-0004] Clinical research is the frontline of medical innovation. Through research projects, scientists and physicians make medical breakthroughs that directly impact the lives of patients and their families. However, what many patients and […]