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Global Harmonization Task Force
Results: 752

#	Item
551	Global Guidance for Adverse Event Reporting for Medical Devices Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:50 Clinical research Health Global Harmonization Task Force Pharmaceutical industry Medical technology Adverse event Medical device Patient safety Postmarketing surveillance Medicine Medical equipment Technology
552	Quality Management System – Medical Devices – Guidance on the Control of Products and Services Obtained from Suppliers Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-26 17:31:12 Medical equipment Quality management Quality Medical technology Supply chain management Global Harmonization Task Force Medical device ISO Supplier evaluation Technology Business Medicine
553	Clinical Investigations Study Group 5 Final Document GHTF/SG5/N3:2010 Clinical Investigations Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:15 Medical equipment Technology Research Medical statistics Global Harmonization Task Force Clinical trial ISO 14155 Medical device Regulatory requirement Pharmaceutical industry Clinical research Medicine
554	GHTF Guiding Principles GHTF Steering Committee Final Document GHTF/SC/N1R8:2005 May 20, 2005 Page 1 of 7 GHTF/SC/N1R8:2005 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-14 00:35:13 GMDN Medical equipment Global Harmonization Task Force Medical device
555	Clinical Evidence for IVD Medical Devices - Novmeber 2012 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:53:16 Science Pharmaceutical industry Global Harmonization Task Force Medical technology Food and Drug Administration Medical device IVD Clinical trial Validity Medicine Health Medical equipment
556	GHTF/SG1/N70:2011 FINAL DOCUMENT Global Harmonization Task Force Title: Label and Instructions for Use for Medical Devices Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:39 Global Harmonization Task Force Medical technology Health Food and Drug Administration Medical device Pharmaceutical industry Unique Device Identification Verification and validation Medical equipment Medicine Technology
557	GHTF SG2 N61R3: PMS Harmonisation Chart SG2 WD GHTF SG2 N61R3: PMS Harmonisation Chart SG2 WD Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:51 Health Global Harmonization Task Force Medical device Clinical trial Surveillance Medical equipment Medicine Technology
558	GHTF/SG2/N6 R3:2002 August 28, 2000 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:51 Pharmacology Pharmaceutical industry Medical equipment Clinical research Adverse event Medical device Federal Food Drug and Cosmetic Act Global Harmonization Task Force MedWatch Medicine Health Food and Drug Administration
559	GHTF Operating Procedures GHTF Steering Committee Final Document GHTF/SC/N3R11:2010 GHTF Operating Procedures Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-14 00:35:14 Global Harmonization Task Force Politics Medical device Document management system Portable Document Format Public comment Committee Medical equipment Medicine Technology
560	GHTF SG1 Standards in Assessment of Medical Devices - March 2008 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:34 Medical technology Global Harmonization Task Force Standards Medical device American National Standards Institute Conformity assessment GMDN Medical equipment Medicine Technology

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