Form FDA 1572 is the contract between the clinical investigator and the federal government assuring that he or she will comply with the FDA regulations 21 CFR 312.53 ... potentially bias a clinical ...

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems" training has ... companies must meet US FDA 21 CFR 820 (The QSR ...

The new dietary and food supplements GMP certification program is designed to support industry players to achieve regulatory compliance in the United States.