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).
IRB Responsibilities: Investigator Qualifications, Adequacy of Sites, and IND/IDE Requirement Determination Per the August 2013 FDA Guidance
January 15 | Registration Deadline January 14
Physician: Manage your Career Effectively!
January 22 | Registration Deadline January 21
Preparing for an FDA Audit
January 29 | Registration Deadline January 28
2012 Inspection Findings Related to the Informed Consent Procedure: Lessons Learned
February 12 | Registration Deadline February 11
How to Navigate the Pathway from Study Coordinator to CRA
February 19 | Registration Deadline February 18
Update on FDA Refuse to Accept (RTA) Policy for 510(k): Refusals and Emerging Strategies
February 26 | Registration Deadline February 25
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.