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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
Results: 311

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11	News Release 25th IFPMA Assembly in Washington DC Explores Theme of “A Shared Commitment to Global Health” Washington DC, 10 November 2010 – The International Federation of Pharmaceutical Manufacturers & Associatio Add to Reading List Source URL: www.jpma.or.jp Language: English - Date: 2013-06-30 20:56:25 Medicine Pharmacology Clinical research IFPMA Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Novartis International AIDS Vaccine Initiative Clinical trial Pharmaceutical sciences Health Pharmaceutical industry
12	News Release R&D Pharmaceutical Industry Emergency Aid for Haiti Emergency Cash and Medicine Donations already amount to more than USD 16.9 million Geneva, 19 January 2010 – The research-based pharmaceutical industry r Add to Reading List Source URL: www.jpma.or.jp Language: English - Date: 2013-06-30 20:56:17 Pharmacology Pharmaceuticals policy Clinical research IFPMA International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use AmeriCares Direct Relief International Novartis Clinical trial Pharmaceutical sciences Health Pharmaceutical industry
13	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmaceuticals policy Health Pharmaceutical industry Drug discovery Clinical trial International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Regulatory requirement Food and Drug Administration Pharmaceutical sciences Clinical research Research
14	Microsoft Word - E2BR3_Implementation_Working_Group_Questions_and_Anwers_ver1.00.docx Add to Reading List Source URL: estri.org Language: English - Date: 2015-01-27 12:31:00 Medical informatics Standards organizations Health informatics Computer file formats Health Level 7 XML Schema XML International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Computing Health OSI protocols
15	ICH eCTD Specification Change Control V1.8 ICH eCTD Specification Change Control V1.8 ICH eCTD Specification Change Control V1.8 ICH eCTD Specification Change Control V1.8 ICH eCTD Specification Change Control V1.8 ICH e Add to Reading List Source URL: estri.org Language: English - Date: 2012-06-05 01:13:00 Drug safety Standards Medical informatics Electronic Common Technical Document Medicine Technology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Change control Specification Clinical research Research Clinical Data Management
16	IFPMA Ethical Promotion - Issues Brief Add to Reading List Source URL: www.jpma.or.jp Language: English - Date: 2013-12-02 01:17:39 Pharmacology Research Clinical research IFPMA International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical trial Pharmaceutical marketing Pharmaceutical sciences Pharmaceutical industry Pharmaceuticals policy
17	Tool for international collaboration in guideline development Add to Reading List Source URL: www.ha-ring.nl Language: English - Date: 2013-07-19 19:23:18 Evidence-based medicine Medical guideline Medical literature Guidelines International Network Evaluation National Collaborating Centre for Mental Health International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Medicine Health Medical informatics
18	25 SeptemberEMA/CHMPCommittee for Medicinal Products for Human Use (CHMP) Assessment report Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2014-12-17 05:29:48 Research Drug safety Pharmacology European Medicines Agency Pharmaceuticals policy Committee for Medicinal Products for Human Use International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacovigilance Serious adverse event Clinical research Pharmaceutical sciences Pharmaceutical industry
19	PRESS RELEASE Lisbon, Portugal, ICH MedDRA® Management Board Meeting ICH MedDRA Management Board Endorses Blue Ribbon Panel Recommendation for a 27th SOC Lisbon, 9 November 2014 – The ICH MedDRA Management Board met i Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-11-18 02:20:15 Research MedDRA Drug safety World Health Organization Health Medicine International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Council for International Organizations of Medical Sciences Henry Dunant Pharmaceuticals policy Clinical research Pharmacology
20	Final Concept Paper M4E(R2): Enhancing the Format and Structure of Benefit-Risk Information in ICH M4E(R1) Guideline Revised on 23 March 2015 Endorsed by the ICH Steering Committee on 27 March 2015 Add to Reading List Source URL: www.ich.org Language: English - Date: 2015-04-14 09:36:09 Pharmaceuticals policy Management Safety Actuarial science Ethics Environmental Working Group Risk Clinical research Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use