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and Cosmetic Act
Results: 5012

#	Item
591	07.__H130005.A002_APPROVAL_ORDER[removed]pdf Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-22 15:51:34 Technology Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medical device Title 21 of the Code of Federal Regulations Adverse event Humanitarian Device Exemption Unique Device Identification Food and Drug Administration Medicine Health
592	FAP_LabScientist_raw_km_RF.jpg Add to Reading List Source URL: www.pewtrusts.org Language: English - Date: 2014-03-12 11:44:53 Food and Drug Administration Food law Food safety Food additives Adulteration Generally recognized as safe Federal Food Drug and Cosmetic Act Food contact materials Food Safety Modernization Act Food and drink Health Safety
593	Protecting the U.S. Food Supply U.S. Food and Drug Administration U.S. Department of Health and Human Services Add to Reading List Source URL: seafood.oregonstate.edu Language: English - Date: 2013-09-03 14:06:36 Medicine Food law Pharmacology Pharmaceuticals policy Adulteration Dietary supplement Federal Food Drug and Cosmetic Act Center for Food Safety and Applied Nutrition Food Safety and Modernization Act Food and Drug Administration Food and drink Health
594	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
595	FDA’s Home Use Medical Device Initiative Add to Reading List Source URL: www.fda.gov Language: English Technology Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Center for Food Safety and Applied Nutrition Office of Regulatory Affairs Adverse event Unique Device Identification Premarket approval Food and Drug Administration Medicine Health
596	Handbook 130 – 2014 NCWM Policy, Interpretations, and Guidelines VI. NCWM Policy, Interpretations, and Guidelines, Section 2 Excerpts from NCWM Publication 3 Add to Reading List Source URL: www.nist.gov Language: English - Date: 2013-10-25 16:37:16 Business Science Industrial design Packaging and labeling Retailing Fair Packaging and Labeling Act Food and Drug Administration International Nomenclature of Cosmetic Ingredients Technology Packaging Industrial engineering
597	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-06 09:57:10 Health Food law Pharmaceuticals policy Medical equipment Medical device Medical technology Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Technology
598	Federal Register / Vol. 75, No[removed]Thursday, August 26, [removed]Notices The Food and Drug Administration (FDA) is issuing an order under the Federal Food, Drug, and Cosmetic Act (the act) debarring Su Van Ho for a peri Add to Reading List Source URL: www.atsdr.cdc.gov Language: English - Date: 2012-02-23 13:39:07 Agency for Toxic Substances and Disease Registry Environment of the United States Food and Drug Administration Food law Adulterated food Federal Food Drug and Cosmetic Act United States Department of Health and Human Services United States Public Health Service Health Medicine
599	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
600	[removed]Federal Register / Vol. 79, No[removed]Tuesday, September 9, [removed]Notices Leroy A. Richardson, Chief, Information Collection Review Office, Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-10-07 13:05:58 Pharmaceutical sciences Pharmaceuticals policy Food law Therapeutics United States Public Health Service Federal Food Drug and Cosmetic Act Animal drugs Abbreviated New Drug Application Prescription Drug User Fee Act Food and Drug Administration Medicine Health

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