Are you looking for improvements or expert advice in:

1. Implementing purchasing controls per FDA 21 CFR 820.50 including effective global supplier management?
2. CAPA system management per FDA 21 CFR 820.100?
3. Improving your medical device complaint handling process per FDA 21 CFR 820.198?
4. Developing and transferring production technology on a global basis? Need support with validations or manufacturing/process engineering?
5. Supporting your program/project management initiatives?
6. Resolving biosensor (optical or electro-chemical disposable strip) product, process, or manufacturing issues?