The table below provides a convenient way to search for FDA guidance documents from a single location. You can search for documents using key words, and you can narrow or filter your results by product, date issued, FDA organizational unit, type of document, subject, draft or final status, and comment period start and end dates. If you are looking for recently issued guidances, this table by default is sorted by ‘issue date’.In addition to the search features within the table, you can also browse collections of guidance documents by topic below. 

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Product Animal & Veterinary Biologics Cosmetics Dietary Supplements Drugs Food & Beverages Medical Devices Radiation-Emitting Products Tobacco

FDA Organization Center for Biologics Evaluation and Research Center for Devices and Radiological Health Center for Drug Evaluation and Research Center for Tobacco Products Center for Veterinary Medicine Human Foods Program National Center for Toxicological Research Office of Inspections and Investigations Office of Regulatory Affairs Office of the Commissioner

Topic Administrative / Procedural Adverse Event Reporting Advertising Advisory Committees Animal Rule Antimicrobial Resistance Aquaculture Artificial Intelligence Biopharmaceutics Biosimilars Biostatistics Biotechnology Bovine Spongiform Encephalopathy (BSE) Cellular & Gene Therapy Chemistry, Manufacturing, and Controls (CMC) Clinical - Antimicrobial Clinical - Medical Clinical - Pharmacology Combination Products Compliance Compounding Current Good Manufacturing Practice (CGMP) Digital Health Drug Competition Action Plan Drug Development Tools Electronic Submissions Emergencies Environmental Safety Export FDA Amendments Act (FDAAA) FDA Reauthorization Act of 2017 (FDARA) FDA Safety and Innovation Act (FDASIA) Food and Beverage Safety Food & Drug Administration Modernization Act of 1997 Food Safety Modernization Act (FSMA) Generic Drugs Good Clinical Practice (GCP) GUDID Human Food Safety ICH-Efficacy ICH-Multidisciplinary ICH-Quality ICH-Safety Import Ingredients Inspection International Investigation & Enforcement Investigational Device Exemption (IDE) Labeling Microbiology Nanotechnology Outbreak Over-the-Counter Packaging Pediatric Product Development Pharmaceutical Quality Pharmacology / Toxicology Postmarket Potential Metal or Chemical Contaminant Premarket Rare Diseases Real World Data / Real World Evidence (RWD/RWE) Recalls Records Registration Safety - Issues, Errors, and Problems Sanitation Technology & Discipline Transportation UDI User fees

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Summary	Document	Issue Date	FDA Organization	regulated product taxonomy hidden	Topic old hidden	Topic	Guidance Status	Open for Comment	Comment Closing Date on Draft	Docket Number	Guidance Type hidden	center taxonomy hidden	regulated product parent taxonomy hidden