1. Labeling reviewing, approval and auditing, including warehouse re-labeling activities, to ensure labeling meet CFDA's requirements.
2. Supplier initial approval and distributor periodically review.
3. GSP master data maintenance.
4. Medical Device industry Adverse Event reporting, maintain MD distributor licenses.
5. Monitor post market regulatory trends in Medical Device industry, coordinate CFDA's audits.
6. Influence,communicate and coordinate with Standard Committee of some Vertical Markets, including but not limited to Food Safety, Environment, Pharma/Biopharma...