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- Abbreviations and Acronyms
- About CVM
- Adverse Drug Experience (ADE) Reports
- Advertising
- Advisory Committee
- ADUFA (Animal Drug User Fee Act)
- Animal Drug Approval
- Animal Drug Availability Act (ADAA)
- Animal Drugs for Minor Uses and for Minor Species
- Animal Drug Products Online Database System (FDA Approved)
- Animal Drug User Fee Act (ADUFA)
- Animal Feed
- Animal Medicinal Drug Use Clarification Act (AMDUCA)
- Animal Testing
- Animal Waste
- Animation - Antimicrobial Resistance
- Annual Reports
- Anthelmintics
- Anticaking Agents
- Antimicrobial Resistance
- Aquaculture
- Biotechnology
- Bioterrorism
- Bovine Spongiform Encephalopathy (BSE)
- Bovine Somatotropin (BST)
- BSE Inspections
- Budget
- Cats
- Clinical Investigators
- Cloning
- Codex Activities
- Commissioned Corps Veterinary Category
- Compliance Policy Guides (CPG) Manual
- Compounding
- Conferences
- Consumer Information
- Consumer Roundtable
- Contacting CVM
- Cooperative Research and Development Agreements (CRADA)
- Counterterrorism
- Current Good Manufacturing Practices (cGMP)
- Current Labels
- CVM Memos
- CVM Updates
- CVM Updates - e-Mail List Subscription
- Database - BSE Inspections
- Database - FDA Approved Animal Drug Products
- "Dear Doctor" Letters
- Devices (Veterinary)
- Dioxin
- Dogs
- Drug Approval (Animal)
- Drug Information Laboratory
- Education - Food Safety
- Educational Materials
- Animation - Antimicrobial Resistance
- Annual Reports
- Brochures
- Judicious Use
- NARMS | text | | pdf |
- Pharmacoviligence (pdf)
- FDA and the Veterinarian
- FDA Just the Facts: Safeguarding Animal Health to Protect Consumers
- FDA Veterinarian Newsletter
- Information for Consumer Flyers
- Program Policy and Procedures Manual
- Spanish Language Publications
- Videos
- Electronic Submissions
- e-Mail List – CVM Updates
- Employee Telephone Listing
- Employment Opportunities
- Environmental Assessments
- Environmental Assessment Technical Handbook
- Español - Publicaciones
- Exporting - Animal Feed
- Extra-Label Animal Drug Use
- FAQ's (Frequently Asked Questions)
- FDA and the Veterinarian
- FDA Approved Animal Drug Products Online Database System
- FDAMA (FDA Modernization Act of 1997)
- FDA Codex Activities
- FDA Talk Papers
- FDA Veterinarian Newsletter
- Federal Register Notices
- Feed Contaminants
- Feed Ingredients
- Feed Mill Licensing
- Fish
- Food Additives/Food Additive Petitions - Animal Feed
- Food Facility Registration
- Food Safety Initiative
- Forms
- Framework Document
- Freedom of Information Act (FOIA)
- Freedom of Information Summaries (FOI'S)
- The Federal Food, Drug, and Cosmetic Act
- Fumonisins
- Generic Animal Drug and Patent Term Restoration Act (GADPTRA) Policy Letters
- Genetically Engineered Plants/Animals
- Green Book
- Guidance Documents and Guidelines
- Import Alerts
- Importing - Animal Feed
- Importing - Veterinary Drugs
- Information and Requirements For New Animal Drug Approval
- Information For Consumers
- Intern Programs
- Laws or Regulations Applicable to or Administered by CVM
- Current Labels
- Leveraging--Collaborating with Stakeholders
- Master Files
- Medical Devices(Veterinary)
- Medicated Feed Mill Licensing
- Meetings
- Memos
- Minor Species Minor Uses (MUMS)
- Monkeypox
- National Antimicrobial Resistance Monitoring System (NARMS)
- NARMS Brochure - English Language
- NARMS Brochure - Spanish Language
- New Animal Drug Application Page
- News Releases -HHS/FDA
- Notice of Claimed Investigational Exemption ("NCIE") Electronic
Submissions- Notice of Opportunity for Hearing (NOOH)
- Notice of Regulatory Activity Letters to Pharmaceutical Companies
- Parasites
- Pet Foods
- Pharmaceutical Good Manufacturing Practices (GMPs)
- PHS Commissioned Corps Veterinary Category
- Piperazine
- Prior Notice
- Product Safety Information
- Program Policy and Procedures Manual Index
- Prudent Use of Antimicrobials
- Publicaciones - Español
- Publications - Spanish
- Public Meetings (Antimicrobial Resistance)
- Rabbits
- Regulatory Activity Letters to Pharmaceutical Companies (Notice of)
- Requirements of Laws and Regulations Enforced bythe U.S. Food and Drug Administration
- Research
- Resistance (Antimicrobial)
- Risk Assessment Document
- Risk Assessment Document (Draft)
- Roundtable