FDA Clinical Trial Requirements, Regulations, Compliance and GCP Virtual Conference
This three-day virtual conference is intended to share information among FDA representatives and the regulated community, to facilitate the understanding of regulations, guidelines and practices, and to suggest methods and opportunities to enhance the research professional’s product development experience. The program will focus on the relationships among the FDA and clinical trial staff, investigators and IRBs. The sessions will highlight three areas that present challenges to sponsors and investigational sites: FDA Clinical Research Requirements, Enhancing Success through Communication and Financial Incentives, and Assuring Confidence in Clinical Research.
November 17 to 19, 2020
11:00 am to 4:15 pm ET*
*All times in Eastern Time Zone
Standard Rate - Member Fee - $100
Standard Rate - Non-Member Fee *- $175
Federal Government Employee Rate - Member Fee - $75
Federal Government Employee Rate - Non-Member Fee*- $150
FDA Employee Rate - FEE WAIVED
* Non-Member Fees include a non-refundable one-year membership in SOCRA
SOCRA designates this educational activity for a maximum of 11.25 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 11.25 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
CME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
CNE for Nurses: Society of Clinical Research Associates is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center's Commission on Accreditation.