Global Harmonization Task Force

Results: 752



#Item
501Health / Food and Drug Administration / Medical technology / Medical device / Premarket approval / Global Harmonization Task Force / Professional certification / Medicine / Technology / Medical equipment

Untitled Document This content was archived on June 24, 2013. Archived Content Information identified as archived on the Web is for reference, research or recordkeeping purposes. It

Add to Reading List

Source URL: hc-sc.gc.ca

Language: English - Date: 2013-07-09 16:55:11
502Technology / Medical technology / Global Harmonization Task Force / Health informatics / GMDN / Medical device / Pharmacology / Food and Drug Administration / Nomenclature / Medicine / Medical equipment / Health

APEC Harmonization Center 2011 AHC Workshop on Medical Devices: “Implementation of GHTF Documents” Understanding Japanese Medical Device Requirements

Add to Reading List

Source URL: www.pmda.go.jp

Language: English - Date: 2012-06-18 00:45:45
503Health / Medical equipment / Clinical research / Drug safety / Pharmaceutical industry / Global Harmonization Task Force / Good Laboratory Practice / Pharmacovigilance / Eucomed / Medicine / Pharmaceutical sciences / Pharmacology

ICDRA Workshop I Consideration on Global Harmonization Oct. 25, 2012 Dr. Nobumasa Nakashima

Add to Reading List

Source URL: www.pmda.go.jp

Language: English - Date: 2012-11-15 19:10:08
504Health / Quality management / Quality / Pharmaceuticals policy / Global Harmonization Task Force / Pharmaceutical industry / Food and Drug Administration / Medical device / Regulatory affairs / Medicine / Technology / Medical equipment

ELISABETH M GEORGE Education  Northeastern University Boston, MA Masters Certificate in Engineering Management

Add to Reading List

Source URL: www.fda.gov

Language: English
505Research / Clinical research / Pharmaceutical industry / Drug safety / Pharmacovigilance / Pharmacy / Global Harmonization Task Force / Clinical trial / Good Clinical Practice / Pharmacology / Pharmaceutical sciences / Health

国際部紹介資料(英語版)

Add to Reading List

Source URL: www.pmda.go.jp

Language: English - Date: 2014-03-14 02:20:05
506Pharmaceutical industry / Clinical research / Medical equipment / Pharmaceuticals policy / Medicines and Healthcare products Regulatory Agency / European Medicines Agency / Global Harmonization Task Force / United States Pharmacopeia / Package insert / Pharmaceutical sciences / Medicine / Pharmacology

PMDA Updates October, 2010 < NEWS> 1) Confidentiality Arrangement with MHRA : October 14, 2010 The Medicines and Healthcare Products Regulatory Agency (MHRA) of the United Kingdom of Great Britain and Northern Irelan

Add to Reading List

Source URL: www.pmda.go.jp

Language: English - Date: 2010-11-19 01:45:28
507Quality management / Medical technology / Quality / Pharmaceutical industry / Global Harmonization Task Force / Corrective and preventive action / Quality management system / ISO 13485 / Medical device / Technology / Medicine / Medical equipment

Medical device QMS/GMP system and audit

Add to Reading List

Source URL: www.pmda.go.jp

Language: English - Date: 2012-06-18 00:45:53
508Pharmacology / Patient safety / Medical terms / Medical device / Medical technology / Global Harmonization Task Force / Food and Drug Administration / Regulatory requirement / Health Canada / Medicine / Health / Medical equipment

Microsoft Word - Medical Devices Program Evaluation Final Report Feb 2014.docx

Add to Reading List

Source URL: hc-sc.gc.ca

Language: English - Date: 2014-07-08 13:48:26
509Medical technology / Global Harmonization Task Force / Medical device / Clinical research / Pharmaceutical industry / IVD / Documentation / Quality management system / Validation / Medical equipment / Technology / Medicine

Summary Technical Documentation (STED) for Demonstrating Conformity to the Essential Principles of Safety and Performance of In Vitro Diagnostic Medical Devices

Add to Reading List

Source URL: www.imdrf.org

Language: English - Date: 2012-11-13 17:52:37
510Medical equipment / Global Harmonization Task Force / Medical device

Medical Devices: Post Market Surveillance: National Competent Authority Report Exchange Criteria GHTF/SG2/N20R10:2002 Study Group 2 – Final Document GHTF/SG2/N20R10:2002

Add to Reading List

Source URL: www.imdrf.org

Language: English - Date: 2012-11-13 17:52:52
UPDATE