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Clinical research / Health / Drug safety / Pharmacy / Summary of Product Characteristics / Directive 2001/83/EC / Pharmacovigilance / Supplementary protection certificate / Qualified Person for Pharmacovigilance / Pharmaceuticals policy / Pharmaceutical sciences / Pharmacology


Microsoft Word - Chap 2 rev 2007 Feb 14 clean fin.doc
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Document Date: 2013-10-09 09:37:50


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City

Athens / Brussels / /

Company

Mutual Recognition Facilitation Group / CMD(h) The Mutual Recognition Facilitation Group / /

Country

Poland / Hungary / Estonia / Slovenia / Malta / Lithuania / Cyprus / Latvia / Czech Republic / /

Event

Product Issues / Product Recall / /

IndustryTerm

pharmaceutical form / Generic medicinal products / reference medicinal product / biotechnology process / rDNA technology / biotechnology step / informal / reference product / homeopathic products / subsequent applications / medicinal product / human medicinal products / human medicinal product / withdrawn medicinal product / treatment of certain diseases / medicinal products / coordination / orphan medicinal products / herbal medicinal products / manufacturing process / /

MedicalCondition

certain diseases / CMD / tiredness / /

Organization

Mutual Recognition EUROPEAN COMMISSION ENTERPRISE DIRECTORATE / Mutual Recognition CHAPTER / Pharmacovigilance Working Party / See Chapter / European Union / Pharmaceutical Committee / Council of the European Union / Committee for Human Medicinal Products / /

Position

Vice-chairperson / chairperson of the coordination group / representative / General / /

Product

However / /

ProgrammingLanguage

EC / /

Technology

biotechnology / http / rDNA technology / /

URL

http /

SocialTag