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1	LSNE Contract Manufacturing has two cGMP facilities located in New Hampshire capable of producing reagents, diagnostics and medical device components and products. Add to Reading List Source URL: www.lyophilization.com Language: English - Date: 2013-01-25 02:43:04 Pharmaceutical industry Food preservation Freeze-drying Food and Drug Administration Validation QSIT Pharmaceutical sciences Manufacturing Food and drink
2	QSIT Presentation - May 2002 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:06 Quality management system QSIT Food and Drug Administration Form FDA 483 Ø
3	FDA’s Home Use Medical Device Initiative Add to Reading List Source URL: www.fda.gov Language: English Technology Office of Regulatory Affairs QSIT Federal Food Drug and Cosmetic Act Medical device Office of Criminal Investigations Regulatory affairs Form FDA 483 Good manufacturing practice Food and Drug Administration Medicine Health
4	Microsoft Word - DV201 Basic Medical Device Course Announcement December[removed]doc Add to Reading List Source URL: www.fda.gov Language: English Technology Clinical research Pharmaceutical industry Therapeutics United States Public Health Service QSIT Validation Medical device Medicine Food and Drug Administration Pharmaceutical sciences
5	Microsoft Word - DV201 Basic Medical Device Course Announcement March 4-15 2013amended.doc Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Therapeutics United States Public Health Service QSIT Validation Food and Drug Administration Pharmaceutical sciences Research
6	FDA’s Home Use Medical Device Initiative Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Office of Regulatory Affairs QSIT Federal Food Drug and Cosmetic Act Medical device Regulatory affairs Office of Criminal Investigations Form FDA 483 Good manufacturing practice Food and Drug Administration Medicine Health
7	Pilot Multipurpose Audit Program (PMAP) Questions and Answers related to the Pilot Q1 What is the purpose of the Pilot Multipurpose Audit Program (PMAP)? Add to Reading List Source URL: www.fda.gov Language: English Business Auditing Pharmaceutical industry Food and Drug Administration Validity Audit Quality management system QSIT Information technology audit Accountancy Medicine Quality management
8	Microsoft Word - 1- CP[removed]Coversheet February[removed]Final.doc Add to Reading List Source URL: www.fda.gov Language: English Technology Good manufacturing practice Form FDA 483 Center for Devices and Radiological Health Medical device Design controls Quality management system QSIT Title 21 of the Code of Federal Regulations Food and Drug Administration Medicine Health
9	Microsoft Word - Basic Medical Device Course Announcement March[removed]_2_.doc Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Clinical research Pharmacology United States Public Health Service QSIT Validation Food and Drug Administration Pharmaceutical sciences Research