EN PL
  1. www.sciencepharma.com
  2. News
  3. Clinical/Medical
  4. EMEA: Dossier requirements for Post-authorisation submissions in the centralised procedure

EMEA: Dossier requirements for Post-authorisation submissions in the centralised procedure

30.01.2009
EMEA:
Dossier requirements for Post-authorisation submissions in the centralised procedure from 01 January 2009. Dossier requirements for (Co-) Rapporteur and CHMP members.
The source of the news: http://www.emea.europa.eu/pdfs/human/regaffair/30033908en.pdf