HKBIO US-FDA Medical Device Regulations Seminar, Hong Kong

April 21, 2015

The HKBIO US-FDA’s Medical Device Regulations Seminar was organized by Hong Kong Biotechnology Organization (HKBIO); sponsored by Lee’s Pharmaceutical Holdings Limited, Powder Pharmaceuticals Incorporated and Hong Kong Science and Technology Parks Corporation (HKSTP), and held in Hong Kong Science Park on April 21, 2015. . We invited Mr. Francis John Eng (ex-FDA Investigator from 1972-2014) to give a training seminar regarding US FDA’s Medical Device regulations, primarily covering 21 CFR 803 and 21 CFR 820, including the following topics:

- QSR / GMP
- CAPA
- Risk Management
- MDRs
- US FDA Inspections in China

To download the slides of the seminar, please click here.

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