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ISO 4
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#	Item
621	Training Modules on General Food Safety Plans for the Food Industry Section 3-4: Principle 2: Identify Critical Control Points Add to Reading List Source URL: fscf-ptin.apec.org Language: English - Date: 2013-02-11 16:05:29 Risk Food safety Safety engineering Occupational safety and health ISO 22000 Chemical engineering Hazard analysis and critical control points Critical control point Asia-Pacific Economic Cooperation Safety Management Hazard analysis
622	TDMS No[removed]Test Type: 90-DAY E04: MEAN BODY WEIGHTS AND SURVIVAL TABLE Ethanone, 1-(1,2,3,4,5,6,7,8-Octahydro-2,3,8,8-Tetramethyl-2-Naphthalenyl)- (Iso-E Add to Reading List Source URL: ntp.niehs.nih.gov Language: English - Date: 2014-11-11 13:00:53 Ajax Web development software Wt Software World Wide Web Web development
623	NATIONAL BOOKING REPORTING SYSTEM DATA WAREHOUSE DATA DICTIONARY Version 1.4 July 2006 Add to Reading List Source URL: www.health.govt.nz Language: English - Date: 2014-11-26 14:53:19 Metadata Metadata registry Data management Business Data warehouse Information technology management ISO/IEC 11179 Performance indicator Business intelligence Data Information
624	Study Group 4: auditing. Guidelines for regulatory auditing of quality systems of medical device manufacturers: General requirements: [removed]Final document Study Group 4: auditing. Guidelines for regulatory auditin Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:08 Business Audit Environmental audits Quality audit Information technology audit ISO Information technology audit process Software audit review Auditing Accountancy Risk
625	Guidelines for Regulatory Auditing of Quality Management Systems of Medical Device Manufacturers Part 3: Regulatory Audit Report SG4 N33 R10 – Study Group 4 – Working Draft Guidelines for Regulatory Auditing of Qual Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:10 Risk Audit Global Harmonization Task Force Information technology audit ISO Information technology audit process Financial audit Auditing Accountancy Business
626	Guidelines for Regulatory Auditing of Quality Management Systems of Medical Device Manufacturers Part 2: Regulatory Auditing Strategy GHTF/SG4(PD)/N30R16:2005 – Study Group 4 – Proposed Document Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:09 Evaluation Technology Quality Medical equipment Information technology audit ISO Audit Quality audit Quality management system Quality management Auditing Business
627	Study Group 4: Auditing. Guidelines for regulatory auditing of quality systems of medical device manufacturers: part 2: language requirements: [removed]Proposed document Study Group 4: Auditing. Guidelines for regu Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:08 Auditing Global Harmonization Task Force Health Pharmaceutical industry Pharmaceuticals policy Medical device Documentation Title 21 CFR Part 11 ISO Medical equipment Medicine Technology
628	Guidelines for Regulatory Auditing of Quality Management Systems of Medical Device Manufacturers Part 2: Regulatory Auditing Strategy GHTF/SG4/N30R20:2006 – Study Group 4 – Final Document Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:10 Evaluation Technology Quality Medical equipment Information technology audit ISO Audit Quality audit Quality management system Quality management Auditing Business
629	Study Group 4 “Regulatory Auditing“ Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:58 SG postcode area Audit ISO 13485 Medical device Districts of England Counties of England Geography of England Medical equipment Medical technology Global Harmonization Task Force
630	Canberra Meeting minutes.doc Page 2 of 4 GHTF SG 3 Meeting Minutes Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:57 Medical technology Management Quality Global Harmonization Task Force Corrective and preventive action Quality management system ISO 13485 Medical device Therapeutic Goods Administration Medicine Technology Medical equipment

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