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Electronic common technical document
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111	Microsoft Word - eCTD Implementation Survey Report-v2.0.doc Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-06-08 09:29:22 Medical informatics Electronic Common Technical Document Medicine Clinical research Clinical Data Management Research
112	PRESS RELEASE Lisbon, Portugal, November 2014 The International Conference on Harmonisation (ICH) Steering Committee (SC) and its Expert Working Groups (EWGs) met in Lisbon, Portugal, EU on November 8 – 13, 2014. The m Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-12-02 06:07:25 Pharmaceuticals policy Pharmaceutical sciences Health Clinical Data Management Pharmacology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document Common Technical Document Good Clinical Practice Clinical research Research Pharmaceutical industry
113	Product Information RLPmanager™ Benefits Maximum flexibility in study creation Add to Reading List Source URL: www.extedo.com Language: English - Date: 2015-04-17 01:12:21 Knowledge Clinical Data Management Pharmacology Medical informatics Electronic Common Technical Document Information technology management Submission management Document management system Portable Document Format Clinical research Research Science
114	ANNEX 2 (< FROM ACTIVE SUBSTANCE MASTER FILE HOLDER ON HEADED PAPER>) Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 06:33:33 Pharmaceutical industry Research Medicine Pharmaceuticals policy Health Clinical research Clinical Data Management Electronic Common Technical Document
115	EX_Gesamtgrafik_2014_17dp.indd Add to Reading List Source URL: www.extedo.com Language: English - Date: 2015-05-07 03:04:29 Knowledge Pharmaceutical sciences Clinical Data Management Medical informatics Drug safety Electronic Common Technical Document Submission management Open Text Corporation Pharmacovigilance Clinical research Research Pharmaceutical industry
116	Benefits llows creation and maintenance A of many child dossiers based on one parent dossier. educes update times for variaR Add to Reading List Source URL: www.extedo.com Language: English - Date: 2015-01-26 08:45:35 Research Knowledge Education Clinical Data Management Medicine Electronic Common Technical Document Submission management Document management system Electronic submission Competitions Digital media Grants
117	eAF-Release-Notes-Variation_1 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2015-05-07 06:59:19 Clinical Data Management Clinical research Electronic Common Technical Document Portable Document Format World Wide Web XML Computing Computer file formats Open formats
118	Recommendation Notebook Version 3.0 ICH M2 Electronic Standards for the Transfer of Regulatory Information Add to Reading List Source URL: estri.ich.org Language: English - Date: 2012-06-04 19:13:02 Environmental Working Group Food and Drug Administration International standard Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical research Research Pharmaceutical sciences
119	Tokyo ICH Symposium: Hot Topics and influence on Asia Add to Reading List Source URL: www.jpma.or.jp Language: English - Date: 2015-01-14 03:33:56 Research Pharmaceuticals policy Pharmaceutics Japan Pharmaceutical Manufacturers Association Pharmacology Pharmacy Electronic Common Technical Document Good Clinical Practice Environmental Working Group Clinical research Pharmaceutical sciences Pharmaceutical industry
120	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE M2 Glossary of Terms and Abbreviations 2 June 2014 Add to Reading List Source URL: estri.ich.org Language: English - Date: 2014-06-13 05:33:24 Pharmaceutical industry Medicine Medical informatics Clinical Data Management Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document IFPMA MedDRA Clinical research Research Health

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