Recent and Proposed Changes in Federal GCP Regulations and Their Impact on How Clinical Research is Conducted
4th Annual Webinar
Tuesday, September 17, 2019
Log in from the convenience of your home or office—Cisco WebEx link will be provided.
Sandra SAM Sather, MS, BSN, CCRA, CCRCVice President, Clinical Pathways, LLC
As part of the continuing efforts to modernize the way we perform clinical trials, there have been some noteworthy GCP federal regulations and guidance changes that directly or indirectly impact all clinical research stakeholders, including sites and sponsors. Attend this webinar to hear about the major categories of change and summary of associated regulations/guidance, including recommendations of an action plan.
Upon completion of this Webcast, attendees should be able to
1. recognize the major federal regulation and guidance changes to GCP
2. discuss how the changes impact clinical trial stakeholders
3. consider what actions might need to be taken for complianceTarget Audience
: All Clinical Research Professionals.Agenda
6:30-6:40 Welcome and Chapter Meeting
6:40-8:00 Educational Program and Q&A
Cost: Complimentary for Chapter Members/$25 Non-MembersRegistration
: Register at Eventbrite
. Log in information will be sent one week prior to the event.Contact hours
: 1.5 Contact hours have been applied for through ACRP. Membership is not required for online registration of contact hours.Contact Hour Cost
: Complimentary for NY Metro Chapter Members/$25 ACRP Members/$25 Non-MembersTo receive contact hours
: Purchase the contact hours on the ACRP NY Metro Chapter website the up to two weeks after the event. After attending the program, log onto the ACRP website between 1-30 days following the event, click “My Courses”, then scroll down to Chapter events to complete the evaluation and receive the online certificate. Membership is not required for online registration/application of contact hours. Click here to purchase contact hours.