Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Dietary Supplement Labeling Requirements and Recommendations Under the Dietary Supplement and Nonprescription Drug Consumer Protection Act FDA More Information…
“FDA released final rules for Foreign Supplier Verification Programs and Accredited Third-Party Certification” FDA More Information…
Use of the Term “Natural” in the Labeling of Human Food Products; Request for Information and Comments FDA More Information…
Investigational New Drug Applications-Determining Whether Human Research Studies Can Be Conducted Without an Investigational New Drug Application; Guidance for Clinical Investigators, Sponsors, and Institutional Review Boards; Partial Stay and Republicati FDA More Information…
FDA’s Strategy for FSMA Training Who Will Provide Training for the Food Industry? Public and Private Partners Working Together FDA More Information…
Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food FDA More Information…
