Interview with Marc Sanchez, Founder of Contract In-House Counsel
It's a constant debate. Pursue a medical device regulatory approval in the US? Or does it make more sense to seek a European approval first? Is there a definitive answer? According to Marc Sanchez, Founder of Contract In-House Counsel, medical device companies would be wise to take a step back and consider the business ramifications first. In this interview with Marc, we learn more about this hotly debated issue as well as a host of other interesting medical device regulatory trends.
So who is Marc Sanchez? He's the Founder of Contract In-House Counsel and Consultants. His law practice focuses on building a regulatory strategy for start-ups and small to midsize companies in the medical device field. This strategy includes both pre-market approval and post-market surveillance matters.
Listen to the "Should Medical Device Companies Pursue Regulatory Approvals in Europe Before the US?" podcast (right click and select "Save Link As" to download the podcast).
Download the PDF Action Points from the "Should Medical Device Companies Pursue Regulatory Approvals in Europe Before the US?" podcast.