International Issues for Medical Device Manufacturers: An Introduction
Examine the legal framework concerning imports and exports of medical devices. Review the basis of approved and unapproved devices. Outline the importation process.
Sarah H. Stec, Senior Counsel, Medical Device Regulatory Law, Johnson & Johnson
This session was recorded as part of FDLI’s Virtual Introduction to Medical Device Law and Regulation Course in April 2020.
- +$100 for nonmembers
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