The Association of Clinical Research Professionals (ACRP) is happy to announce forthcoming updates to several courses in the ACRP catalog. These updates are part of our ongoing efforts to improve engagement and user experience with the courseware.
What’s Happening?
ACRP is updating the design of several courses to provide more-appealing course layouts and improved experiences as users navigate through course content. Changes are not been made to course content or end-of-course assessments. Impacted courses include:
- Investigator Responsibilities
- Implementing a Patient-Centered Informed Consent Process
- Using Metrics to Improve Subject Recruitment and Retention
- Ethics and Human Subject Protection: A Comprehensive Introduction
- Ethics and Human Subject Protection: A Refresher Course
- Improving Recruitment, Accrual, and Retention in Clinical Trials
- Trial Feasibility and Selection Their Impact on Accrual
- ICH Gap Analysis Tool
- Understanding Clinical Trial Protocols: Key Considerations for Effective Development and Feasibility Review
- Mastering Budgeting at Your Site: Building and Negotiating Clinical Trial Budgets that Make Sense
- Form FDA 1572: Get it Right the First Time
- Informed Consent Simulation
What Does this Mean for You?
If you have started but not yet completed any of the above-referenced courses, please complete them by 11:59pm EST on Monday, December 2, or you will be forced to restart the courses when the new versions are launched on Tuesday, December 10.
No action is required if you have already completed these courses and received certificates of completion.
If you have any questions or need additional support, please contact ACRP Customer Care.
Thank you for your continued support of ACRP.