Brief, Focused Learning
Keep pace with regulatory developments and industry trends affecting your clinical trials, or take a deeper exploration of specialized clinical research topics.
These brief, instructor-led, interactive, live online sessions allow you and your team to own your success in clinical research throughout the year — without travel expenses or time away from the office.
ACRP Webinars are accredited to provide 1.5 contact hours/credits (CBRN, ACCME or ACRP) and are just $99 for ACRP Members ($149 Regular).
Before purchasing a Webinar, please review Webinar Frequently Asked Questions (FAQs).
FDA/EMA Inspection Lessons Learned: Essential Document Collection and Retention
May 14 | Registration Deadline May 13
FDA/EMA Inspection Lessons Learned: Protocol Deviations –Why They Occur and How to Handle Them
July 16| Registration Deadline July 15
Setting Your Sites Up for Success: Industry Trends and Best Practices For Sponsors and CROs
August 20| Registration Deadline August 19
FDA/EMA Inspection Lessons Learned: Ineligible Subject Enrollment
September 24 | Registration Deadline September 23
Research Involving Vulnerable Populations
October 8 | Registration Deadline October 7
FDA/EMA Inspection Lessons Learned: Lack of Trial Oversight
October 22 | Registration Deadline October 21
FDA/EMA Inspection Lessons Learned: Communications with IRB/IEC
November 12 | Registration Deadline November 11
You Have Something to Share
Demonstrate your leadership by sharing your knowledge, expertise and experience in clinical research. ACRP is seeking qualified Webinar presenters who are experienced professionals willing to share their knowledge with their fellow clinical research professionals to advance the clinical research enterprise.
ACRP Webinar presenters receive an honorarium, a complimentary registration to a future ACRP Webinar, and the satisfaction of contributing to the betterment of clinical research. Visit Present a Webinar for ACRP for more information about submitting a Webinar proposal.
What is 'Professional Development'? Do You Have a Pathway for Success?
At ACRP, we believe professional development is the intrinsic motivation that comes from within each clinical research professional to recognize his or her responsibility for: safeguarding patient safety; ensuring quality of data; ensuring ethical conduct of clinical trials; ensuring regulatory compliance at all times; and ensuring research projects are completed on time, on target, and on budget.
We support the professional development of clinical research professionals by offering high-quality resources and services that are relevant to the needs, interests, and work of clinical researchers, that are performance-based, and that allow you to own your success in clinical research. And if you're looking for guidance on your professional development, check out ACRP's proprietary Professional Development Pathways for clinical research professionals.
Please visit Professional Development to learn more about how ACRP is supporting the professional growth and development of clinical research professionals, and why ACRP should be your first choice for clinical research training.