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Health / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Electronic Common Technical Document / European Federation of Pharmaceutical Industries and Associations / Pharmaceutical Research and Manufacturers of America / Clinical trial / State Food and Drug Administration / MedDRA / Clinical research / Research / Pharmaceutical sciences


14 November[removed]Public ICH Regional Meeting Public ICH Meeting 14 November 2008
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Document Date: 2012-06-22 05:03:12


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File Size: 259,27 KB

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City

Brussels / /

Company

Pfizer / Fortis / Rapporteur ICH Quality Implementation Working Group / Pharmacopoeias Michael Wierer - EDQM & Pharmacopoeial Discussion Group / Wyeth / AstraZeneca / /

Country

Canada / /

Currency

EUR / /

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Facility

Radisson SAS Hotel / Agence Bascule / /

IndustryTerm

bank charges / art tools / pharmaceuticals / manufacturing / medicinal products / /

Organization

MHRA / ICH Quality Working Groups / Safety Working Party / CHMP-Quality Working Party / European Union / ICH Steering Committee / /

Person

Christine-Lise Julou / Spiros Vamvakas / Kohei Wada / Sabine Brosch / Thomas Lönngren / Mike Ward / Brian Withers / Klaus Olejniczak / David Jones / Joe Cipollina / Peter Arlett / Jennifer Sims Rapporteur / Patricia Mozzicato / Peter Kasper / Beatriz Silva Lima / Jean-Louis Robert / Lois Hinman / Andrew Marr / Robert Baum / Saleh Abdullah Bawazir / Solange Rohou / Anita Colin / /

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Position

Safety Experts Working Groups Session chair / Technical Coordinator / harmonisation priorities Session Chair / Chairman / Executive Director / entire lifecycle Session chair / Director EMEA / Co-Chair / Chair / medicines Session chair / Regional Meeting Session chair / /

Product

M2 / /

Technology

Biotechnology / /

URL

http /

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