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and Cosmetic Act
Results: 5012

#	Item
621	Microsoft Word - Indications for Use Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-06 09:57:12 Health Food law Pharmaceuticals policy Pharmaceutical industry Medical equipment Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Technology
622	Staff Manual Guide[removed] Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Federal Food Drug and Cosmetic Act Animal drugs Office of Regulatory Affairs Form FDA 483 Adulterated food Food and Drug Administration Medicine Health
623	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service __________________________________________________________________________________________________________________________ Food and Drug Administration[removed]N Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-06 09:56:08 Health Medical device Center for Devices and Radiological Health Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Quality management system Code of Federal Regulations Title 21 CFR Part 11 Medicine Food and Drug Administration Technology
624	2012 SUMMARY REPORT On Antimicrobials Sold or Distributed for Use in Food-Producing Animals Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmaceuticals policy Clinical pharmacology Antimicrobial Microbiology Food and Drug Administration Antibiotic resistance Off-label use Federal Food Drug and Cosmetic Act Medicine Health Pharmaceutical sciences
625	Contains Nonbinding Recommendations Guidance for Industry Considerations Regarding Substances Added to Foods, Including Beverages and Dietary Supplements Add to Reading List Source URL: www.fda.gov Language: English Food science Food and Drug Administration Food additives Food safety Food law Dietary supplement Federal Food Drug and Cosmetic Act Center for Food Safety and Applied Nutrition Adulterated food Food and drink Health Safety
626	Guidance for Industry How to Write a Request for Designation (RFD) U.S. Department of Health and Human Services Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceuticals policy Adulteration Pharmacology United States Public Health Service Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Pharmaceutical sciences
627	Guidance for Industry Electronic Submission of Lot Distribution Reports DRAFT GUIDANCE This guidance document is for comment purposes only. Submit one set of either electronic or written comments on this draft guidance b Add to Reading List Source URL: www.fda.gov Language: English Research Structured Product Labeling Center for Biologics Evaluation and Research Adverse Event Reporting System Validation Electronic Common Technical Document Federal Food Drug and Cosmetic Act Abbreviated New Drug Application Title 21 CFR Part 11 Food and Drug Administration Medicine Health
628	LIVE INTERACTIVE LEARNING @ YOUR DESKTOP FDA/NSTA Web Seminar: Teach Science Concepts and Inquiry with Food and Cosmetics Tuesday, May 6, 2008 Add to Reading List Source URL: learningcenter.nsta.org Language: English - Date: 2011-01-04 18:42:05 Medicine Pharmaceutical sciences Food law Skin care Federal Food Drug and Cosmetic Act International Nomenclature of Cosmetic Ingredients Campaign for Safe Cosmetics Cosmetics Food and Drug Administration Health
629	DEPARTMENT OF HEALTH & HUMAN SERVICES April 10, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-13 16:41:56 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology
630	Federal Register / Vol. 79, No[removed]Wednesday, October 1, [removed]Notices designated representatives [42 U.S.C. 9835, Section 640(l)(4)(A)]. Designees must have a letter from the Tribal Government authorizing them to re Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-11-06 11:59:47 Pharmaceuticals policy Pharmaceutical sciences Drug safety Priority review voucher Food law Prescription Drug User Fee Act New Drug Application Federal Food Drug and Cosmetic Act School voucher Food and Drug Administration Medicine Health

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