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Medical device manufacturing
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#	Item
121	FDA Protecting Patients +$100,798,[removed]FTE The following table displays the budget authority and user fees for Protecting Patients in the FY 2011 President’s Budget for FDA programs. FY 2011 Resource Table Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Health Pharmaceuticals policy Pharmacology United States Public Health Service New Drug Application Generic drug Medical device Good manufacturing practice Medicine Pharmaceutical sciences Food and Drug Administration
122	DEVICES AND RADIOLOGICAL HEALTH Introduction FDA’s Devices and Radiological Health Program summarizes the budget program requirements that justify a $285,376,000 request for FY[removed]The Devices and Radiological Health Add to Reading List Source URL: www.fda.gov Language: English Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Mammography Quality Standards Act Medical device Premarket approval Office of Regulatory Affairs Good manufacturing practice Health care in the United States Validation Medicine Food and Drug Administration Health
123	FIELD ACTIVITIES - OFFICE OF REGULATORY AFFAIRS Introduction FDA’s Field Activities – Office of Regulatory Affairs (ORA) Program summarizes the budget program requirements that justify a $546,232,000 request for FY 2 Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Prescription Drug User Fee Act Office of Regulatory Affairs Office of Criminal Investigations Validation Good manufacturing practice Center for Devices and Radiological Health Medical device Food safety Food and Drug Administration Health Medicine
124	Medical Devices A White Paper on Add to Reading List Source URL: www.rmtcnet.com Language: English - Date: 2011-01-27 09:26:30 Technology Center for Devices and Radiological Health Medical device Premarket approval Federal Food Drug and Cosmetic Act Center for Veterinary Medicine Regulatory requirement Good manufacturing practice Adverse event Food and Drug Administration Medicine Health
125	Federal Register / Vol. 68, No[removed]Tuesday, February 25, [removed]Notices VII. When Do I Submit the Fee for Applications Submitted On or After the Date of Publication of This Notice? A. Payment Options for Firms Submitti Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-02-25 06:37:12 Pharmaceutical sciences Health Pharmaceuticals policy Title 21 CFR Part 11 Validation Office of Regulatory Affairs Medical device Good manufacturing practice Unique Device Identification Food and Drug Administration Medicine Pharmaceutical industry
126	Medical Product Supply Chain Safety Report to Congress Dept revisions[removed] Add to Reading List Source URL: www.fda.gov Language: English Quality Pharmaceutical industry Pharmacology Food safety Pharmaceuticals policy Food and Drug Administration Good manufacturing practice Validation Medical device Pharmaceutical sciences Health Medicine
127	Medical Device Manufacturing Pennsylvania offers innovative resources for medical device manufacturers. Its engineering and medical research hubs, along with an evolving advanced manufacturing industry, present an envir Add to Reading List Source URL: www.newpa.com Language: English - Date: 2014-06-26 10:33:44 Manufacturing Harrisburg metropolitan area Harrisburg Pennsylvania Pennsylvania in the American Civil War Medical device Advanced manufacturing Pennsylvania Middle States Association of Colleges and Schools Technology
128	ajh ajh MILLER REPORTING COMPANY, INC. 507 C Street, N.E. Washington, D.C[removed]-6666 Add to Reading List Source URL: www.fda.gov Language: English - Date: 1998-03-12 09:35:35 Clinical pharmacology Food and Drug Administration Pharmacology Therapeutics United States Public Health Service Surveillance Medical device Good manufacturing practice Medicine Health Pharmaceutical sciences
129	industryprofile_MedicalDevices_2013_FINAL.pub Add to Reading List Source URL: www.cerc.com Language: English - Date: 2014-02-07 13:24:09 Covidien Dow Jones Industrial Average Manufacturing Medical device Medicine Medical technology Companies listed on the New York Stock Exchange
130	Our Mandate: To manage and deliver a national compliance and enforcement program for blood and donor semen; cells, tissues and organs; drugs (human and veterinary); medical devices and natural health products, collaborat Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-11-27 10:29:04 Health Pharmaceuticals policy Pharmaceutical industry Clinical pharmacology Active ingredient Abbreviated New Drug Application Good manufacturing practice Medical device Medical prescription Medicine Pharmacology Pharmaceutical sciences

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