Documents
Federal rules and notices from the public comment record, analyzed continuously.
FDA ▾
Citizen Petition from Students for Life of America
3 comments · 1 awaiting analysis
Net support -100% across analyzed comments
Top issues in comments
Citizen Petition from AOOPA DEOLEO and NAOOA
3 comments · 3 awaiting analysis
Analysis in progress
Top issues in comments
How to Prepare a Pre-Request for Designation (Pre-RFD) Guidance for Industry
2 comments · 1 awaiting analysis
Net support +100% across analyzed comments
Top issues in comments
Leveraging Prior Knowledge in the Development of Human Gene Therapy Products Incorporating Genome Editing; Draft Guidance for Industry
2 comments · 1 awaiting analysis
Net support +100% across analyzed comments
Top issues in comments
Psychedelic Drugs: Considerations for Clinical Investigations; Guidance for Industry; Final Guidance
2 comments
Net support 0% across analyzed comments
Top issues in comments
Development of Non-Opioid Analgesics for Chronic Pain; Guidance for Industry; Draft Guidance
2 comments
Net support +50% across analyzed comments
Top issues in comments
- Distinction between addiction and dependence
Citizen Petition from Americans for Scientific Integrity
2 comments
Net support +100% across analyzed comments
Top issues in comments
- Pediatric acetaminophen safety labeling
Guidance for Industry: Questions and Answers on HACCP Regulation for Fish and Fishery Products
2 comments
Net support 0% across analyzed comments
Top issues in comments
- Mixed food storage monitoring
Master Protocols for Drug and Biological Product Development; Guidance for Industry; Draft Guidance
2 comments · 1 awaiting analysis
Net support 0% across analyzed comments
Top issues in comments
- Master protocols guidance
Citizen Petition from Marc Mastrana
2 comments
Net support +100% across analyzed comments
Top issues in comments
Citizen Petition from Robert Naclerio
2 comments
Net support -100% across analyzed comments
Top issues in comments
- Otc access to diphenhydramine
Electronic Submission of Postmarketing Individual Case Safety Reports to the Food and Drug Administration Adverse Event Monitoring System Using International Council of Harmonisation E2B(R3) Data Standards; Regional Data Elements and Implementation Schedule
2 comments
Net support 0% across analyzed comments
Top issues in comments
- Ban nitrous oxide sales