Buffalo, New York, United States •
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About
Business and technical acumen, dynamic presenter, FDA regulatory expert, successful entrepreneur.
FDA oversight for 3D-printed, medical device implants
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.
Building your Medical Device Ecosystem for successful sales
Strategies for designing, funding, and launching new medical devices in the U.S. market. A special emphasis was placed on US FDA requirements.
Changes to the European Union Medical Device Regulations
This presentation discussed new clinical and regulatory requirements necessary to introduce, manufacture and sell medical devices throughout Europe under the MDR - Medical Device Regulations.
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