Getting It Right — Legal Issues to Consider When Choosing Sites in International Clinical Trials
Product Details
Identifying competent and compliance-oriented clinical sites that conform to FDA regulations can be a daunting task.
Where should you go to find the best guidance on the current and emerging legal issues when exploring international clinical research sites?
In this 90-minute Encore presentation, attorney Ann Begley offers her expertise on how to identify clinical sites around the globe that provide the quality and compliance you expect, as well as meet FDA standards — including the agency’s latest final rule on human subject protection standards.
Sign up your entire team to listen in and discover:
- The top three legal issues that are critical when choosing a clinical research site
- Privacy protection
- Litigation risks
- Application of the Foreign Corrupt Practices Act
- What tools are available from the FDA to promote the conduct of clinical trials that comply with U.S. requirements
- Top 10 measures to put into practice to help reduce both legal and regulatory exposure
Register now and get expert guidance on the critical legal issues you need to consider when investigating international clinical trial sites. Plus, you'll get an opportunity to ask your toughest questions during the Q&A session.