Submit Questions and Comments

FDA will aim to respond to general questions about an existing policy, regulation, or the regulatory process that are submitted via email, whenever practicable, within 5 business days or acknowledge receipt of the inquiry and provide an estimated time for response. Questions submitted about specific applications under review will be handled through the product application review process.

• Foods - Industry.Foods@fda.gov
• Cosmetics - Industry.Cosmetics@fda.gov
• Medical Devices - Industry.Devices@fda.gov
• Dietary Supplements - Industry.DietarySupplements@fda.gov
• Radiological Health - Industry.Radiological@fda.gov
• Veterinary Medicine - Industry.Radiological@fda.gov
• Drugs - Industry.Drugs@fda.gov
• Tobacco - Industry.Drugs@fda.gov - or smallbiz.tobacco@fda.hhs.gov (for businesses with fewer than 350 employees)
• Biologics - Industry.Biologics@fda.gov
• Good Clinical Practice - Industry.Biologics@fda.gov
• Combination Products - Industry.Biologics@fda.gov
• Orphan Products - orphan@fda.hhs.gov
• Pediatrics - OPT@fda.hhs.gov
• Advisory Committees - OPT@fda.hhs.gov
• Contact other FDA Offices

Comment on Open Dockets:

FDA Open Dockets on Regulations.gov 

FDA Federal Registers