<--- Back to Details
First PageDocument Content
Pharmacy / Health / Pharmacovigilance / Pharmaceuticals policy / Qualified Person Responsible For Pharmacovigilance / Qualified Person for Pharmacovigilance / Pharmacology / Pharmaceutical sciences / Drug safety
Date: 2013-10-09 09:36:07
Pharmacy
Health
Pharmacovigilance
Pharmaceuticals policy
Qualified Person Responsible For Pharmacovigilance
Qualified Person for Pharmacovigilance
Pharmacology
Pharmaceutical sciences
Drug safety

Comments of the German Medical Association, supported by its Commission on Drugs on the Concept Paper of the European Commission, SANCO Drafting Amendments to Regulation (EC[removed],

Add to Reading List

Source URL: ec.europa.eu

Download Document from Source Website

File Size: 54,57 KB

Share Document on Facebook

Similar Documents

B.08 GUIMA Transfer national requirements AT BE CZ DE(BVL, PEI) EE ES FI FR IE IS IT LT LV NL PL RO SE SK SI UKEMA-CMDv

B.08 GUIMA Transfer national requirements AT BE CZ DE(BVL, PEI) EE ES FI FR IE IS IT LT LV NL PL RO SE SK SI UKEMA-CMDv

DocID: 1rcFm - View Document

COMMISSION OF THE EUROPEAN COMMUNITIES  Brussels, 10 December 2008 SECVolume I

COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 10 December 2008 SECVolume I

DocID: 1qH6O - View Document

Better vigilance for health health protection protection and and innovation

Better vigilance for health health protection protection and and innovation

DocID: 1q6Mb - View Document

Microsoft Word - Volume IX ENdoc

Microsoft Word - Volume IX ENdoc

DocID: 1g2y9 - View Document

Pharmacology / Health / Notary / Drug safety / Qualified Person Responsible For Pharmacovigilance / Marketing authorization / Pharmacovigilance / Public key certificate / Pharmaceuticals policy / Pharmaceutical sciences / Pharmaceutical industry

Name of medicinal product: Procedure number: Module 1: PL=RMS

DocID: 1fB8i - View Document