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Form FDA 483
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#	Item
371	Contains Nonbinding Recommendations Guidance for Industry What You Need to Know About Administrative Detention of Foods Small Entity Compliance Guide Add to Reading List Source URL: www.fda.gov Language: English Medicine Federal Food Drug and Cosmetic Act Food Safety Modernization Act Administrative detention Food safety Center for Food Safety and Applied Nutrition Dietary supplement Detention Form FDA 483 Food and Drug Administration Health Safety
372	Compliance Program Guidance Manual: Program[removed] Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmaceuticals policy Pharmacology Pharmaceutical industry Food law Postmarketing surveillance Form FDA 483 Title 21 CFR Part 11 Center for Drug Evaluation and Research Food and Drug Administration Medicine Health
373	Microsoft Word - Document8 Add to Reading List Source URL: www.fda.gov Language: English Medicine Food and Drug Administration Pharmaceutical industry Pharmaceuticals policy Quality Good manufacturing practice Foodborne illness Generally recognized as safe Form FDA 483 Health Food safety Safety
374	CPGM[removed]Drug Quality Reporting System (DQRS); Medwatch Reports); NDA Field Alert Reports (FARS) Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Research Clinical research Drug safety MedWatch New Drug Application Good manufacturing practice Adverse event Form FDA 483 Food and Drug Administration Pharmaceutical industry Pharmaceutical sciences
375	Microsoft Word - ER321 Attach A JUN 2014.doc Add to Reading List Source URL: www.fda.gov Language: English Medicine Food and Drug Administration Pharmaceutical industry Pharmaceuticals policy Quality Good manufacturing practice Foodborne illness Generally recognized as safe Form FDA 483 Health Food safety Safety
376	General Navigation Guide for Manufacturers of FDA-Regulated Products and Start-ups The general navigation guide below is provided in the event it may be helpful to companies wondering if their planned activities would be Add to Reading List Source URL: www.fda.gov Language: English Center for Food Safety and Applied Nutrition Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medical device Center for Biologics Evaluation and Research Approved drug Dietary supplement Form FDA 483 Unique Device Identification Food and Drug Administration Medicine Health
377	Chapter 11 – Enforcement Statistics Add to Reading List Source URL: www.fda.gov Language: English Medicine Office of Regulatory Affairs FDA Warning Letter Form FDA 483 Center for Food Safety and Applied Nutrition Office of Criminal Investigations Good manufacturing practice Mammography Quality Standards Act Center for Devices and Radiological Health Food and Drug Administration Health Pharmaceutical sciences
378	Microsoft Word - JULY BR301 Course Announcement w_FEMA ID_FINAL v2.doc Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Research Pharmacology Form FDA 483 Clinical trial Clinical investigator New Drug Application Investigational Device Exemption Food and Drug Administration Clinical research Pharmaceutical industry
379	CHAPTER 03 - FOODBORNE BIOLOGICAL HAZARDS Add to Reading List Source URL: www.fda.gov Language: English Food and drink Food law Clinical pharmacology Pharmacology United States Public Health Service Form FDA 483 Center for Food Safety and Applied Nutrition Title 21 of the Code of Federal Regulations ITP Food and Drug Administration Medicine Health
380	REPORT TO CONGRESS First Annual Report on Drug Shortages for Calendar Year 2013 Required by Section 1002 of the Food and Drug Administration Safety and Innovation Act Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences New Drug Application Office of Regulatory Affairs Center for Biologics Evaluation and Research Federal Food Drug and Cosmetic Act Criticism of the Food and Drug Administration Form FDA 483 Food and Drug Administration Medicine Health

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