We will speak at a Strafford webinar providing guidance to life sciences companies and research institutions that are conducting or considering conducting clinical trials outside the United States.

Our panel will address the U.S. and foreign rules and regulations that those considering clinical trials abroad must keep in mind, including Food and Drug Administration (FDA) and federal funding requirements, the Health Insurance Portability and Accountability Act (HIPAA), the Foreign Corrupt Practices Act (FCPA), export laws, and foreign data protection and other laws. The panel will also discuss best practices to mitigate risk and help ensure project success.

The webinar will be held on Wednesday, September 6 from 1:00 – 2:30 p.m. EDT.

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Photo of Clint Hermes Clint Hermes

Clint Hermes draws on his deep experience as general counsel at two teaching hospitals to advise clients on regulatory, accreditation, and corporate governance matters in academic medicine. In addition, Clint also offers clients practical advice and insights on all regulatory and contracting aspects…

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