Michelle Bonn

This was a continuing education course for Attorneys at Phillips Lytle law firm in Buffalo, NY. The information discussed FDA regulatory requirements along with Intellectual property needs for new medical technology.

Strategies for designing, funding, and launching new medical devices in the U.S. market. A special emphasis was placed on US FDA requirements.

This presentation discussed new clinical and regulatory requirements necessary to introduce, manufacture and sell medical devices throughout Europe under the MDR - Medical Device Regulations.