Back to Results
First PageMeta Content
Pharmacology / Clinical research / Drug safety / Pharmacy / Qualified Person Responsible For Pharmacovigilance / Pharmacovigilance / European Medicines Agency / Veterinary Medicines Directorate / Pharmaceutical sciences / Pharmaceuticals policy / Health


EUROPEAN COMMISSION ENTERPRISE DIRECTORATE-GENERAL Single market, regulatory environment, industries under vertical legislation Pharmaceuticals and cosmetics VETPHARM 187
Add to Reading List

Document Date: 2013-10-09 09:25:08


Open Document

File Size: 140,46 KB

Share Result on Facebook

City

Washington DC / Tokyo / Lisbon / London / Brussels / /

Company

VACCINES The Netherlands / Andersen Consulting / Community Reference Laboratories / /

Country

Germany / Switzerland / Netherlands / Italy / Sweden / New Zealand / Belgium / France / Austria / United States / Canada / Australia / Portugal / United Kingdom / Ireland / /

Currency

EUR / /

Event

Product Recall / FDA Phase / Product Issues / Person Communication and Meetings / /

/

IndustryTerm

where no alternative product / rapid solution / veterinary homeopathic products / biotechnology products / joint veterinary/human pharmaceutical committee / veterinary medicinal products / medicinal /biocidal products / medicinal products / manufacturing processes / food / urgent solutions / veterinary pharmaceutical legislation / valid solution / biocidal products / medicinal product / human medicinal products / pharmaceutical committee / web explanatory notes / /

Organization

Telematic Management Committee / Standing Committee / Court of First Instance / World Trade Organization / EUROPEAN COMMISSION ENTERPRISE DIRECTORATE / Codex Committee on Residues of Veterinary Drugs / Immunological Working Party / Numerous Committee / Telematic Steering Committee / Commission Legal Service / EUROPEAN COMMISSION / European Court of Justice / European Union / Pharmaceutical Committee / Steering Committee / Joint Sectorial Committee / /

Person

Cameron McKenna / /

/

Position

Environment Directorate General / consultant / analytical methods The Commission representative / CVMP Chairman / The EMEA representative / marketing authorisation procedure The Commission representative / medicinal /biocidal products The Commission representative / Centralised procedure The EMEA representative / EMEA representative / Chairman / The Commission representative / representative / Enlargement The Commission representative / VICH The EMEA representative / /

Product

period studies / periods / IBR vaccine / /

ProgrammingLanguage

EC / /

ProvinceOrState

Mississippi / /

Technology

biotechnology / draft Protocol / /

SocialTag