Eudra

Title: EudraGMP Registration of Administrator

Eudra Registration Team 18 Send registration confirmation email incl. call no to Eudra Service Desk in order to close call Eudra Registration Team 19 Close call Eudra Service Desk 20 Sign and date the EudraGMP registration form and file it Eudra Registration

www.emea.europa.eu

VICH also on the Web http://vich.eudra.org

VICH International Cooperation on the Harmonisation of Technical Rquirements for the Registration of Veterinary Medicinal Products Introduction What is VICH?

www.aphis.usda.gov

EUDRA CT ( ETHICS COMMITTEE )

Commission europĆ©enne/Europese Commissie, 1049 Bruxelles/Brussel, BELGIQUE/BELGIƋ - Tel. +32 22991111 EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Public Health and Risk Assessment Pharmaceuticals Brussels, 9 November 2010 SANCO/C/8/SF/dn D(2010) 874806 E UDRA CT-LIST OF ...

ec.europa.eu

Frequently Asked Questions relating to the EU Clinical Trials ...

Frequently Asked Questions EU Clinical Trials Register URL: https://www.clinicaltrialsregist er.eu/ Q1. What is the EU Clinical Trials Register? What does it do?

www.clinicaltrialsregister.eu

SUMMARY OF PRODUCT CHARACTERISTICS

... See also "Convention" for format and layout): http://www.emea. eu.int/htms/human/qrd/qrdplt/qrdconvention.pdf , in particular the "Guideline on Summary of Product Characteristics" as published on the Website of the European Commission in the Notice to Applicants, Volume 2C: http://pharmacos.eudra.org ...

apps.who.int

The Committee for Proprietary Medicinal Products (CPMP) held ...

The European Agency for the Evaluation of Medicinal Products Human Medicines Evaluation Unit 7 Westferry Circus, Canary Wharf, London E14 4HB, UK Switchboard: (+44-171) 418 8400 Fax: (+44-171) 418 8551 E_Mail: mail@emea.eudra. org http://www.eudra.org/ emea.html CPMP/960/96 20-11-96 PRESS ...

www.emea.europa.eu

EUDRA GMP MANUAL FOR PUBLIC USERS

European Medicines Agency Communications and Networking U SER M ANUAL FOR P UBLIC USERS 29/06/2009 10:13:07 EudraGMP -Manual for Public Users v0.6, CURRENT 4 1.

eudragmp.ema.europa.eu

LIST OF FIELDS CONTAINED IN THE 'EUDRA CT'

2 1. I NTRODUCTION The Commission, in its Communication regarding the guideline on the data fields contained in the clinical trials database provided for in Article 11 of Directive 2001/20/EC to be included in the database on medicinal products provided for in Article 57 of Regulation (EC) No ...

ec.europa.eu

ICH Guidance for Industry: Q7A Good Manufacturing Practice ...

ICH Guidance for Industry: Q7A Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients

www.fda.gov

EU Module 1 Specification

3 Distribution Version Name Organisation 0.4 http://esubmission.eudra.org 0.7 http://esubmission.eudra.org 0.8 http://esubmission.eudra.org 0.91 0.92 http://esubmission.eudra.org 0.95.1 http://esubmission.eudra.org 0.95.2 http://esubmission.eudra.org 0.95.3 http://esubmission.eudra.org 1.0 http://pharmacos.eudra.org/F2 ...

esubmission.emea.europa.eu

Other sites you could try:

Find videos related to Eudra