North Texas Chapter: Are We Ready for Tomorrow’s Trials (Legally, Professionally & AI)
Event Description:
This program is designed to discuss regulatory updates related to clinical research innovation and AI in the current landscape.
Speakers:
Edye Edens, J.D.
Senior Attorney – Clinical Research
Eeede Life Science Law
The Kulkarni Law Firm/Jenkintown, PA
Presentation: When Protocol Compliance Meets Cybersecurity & Foreign Influence: What Every U.S. Site Needs to Know About the New Risk Landscape
Michele La Badie, ACRP-CP, ACRP-MDP, ACRP-PM
Clinical Trial Manager, Shoulder Innovations
Video Replay Session: Source Data Verification in the Age of AI
David Burrow, PharmD, JD
Director, Office of Scientific Investigations/FDA
Video Replay Session: What’s Next? Clinical Research Innovation
Learning Objectives:
- Discuss what’s next in clinical research innovation
- Discuss current regulatory updates
- Explore how protocol compliance meets cybersecurity & foreign influence under the new risk landscape
Registration Information:
- Chapter Member: $40
- ACRP Member: $40
- Non-Member: $60
- Student: $0
After registering, please visit the event's community page to find the login information or any additional event updates, and to communicate with the event organizer.
The educational portion of this event may be self-reported as 5 points toward an attendee’s Maintenance of Certification. These points are subject to review and acceptance by the Academy of Clinical Research Professionals in accordance with the criteria established. Attendees should keep a record of event participation in case they are randomly selected to participate in the maintenance verification process. The Chapter can provide a certificate of attendance upon request.