First Page | Document Content | |
---|---|---|
![]() Date: 2015-11-08 06:14:30Pharmaceuticals policy Health Medical research Pharmacovigilance European Medicines Agency EudraLex European Directive on Traditional Herbal Medicinal Products Postmarketing surveillance Adverse effect Qualified Person Responsible For Pharmacovigilance EudraVigilance | Add to Reading List |
![]() | 1 AugustElectronic Application Forms are now fully available for use For initial marketing authorisation (human and veterinary), variation and renewal applicationsDocID: 1riM4 - View Document |
![]() | eAF Question and Answers - update-KM_CPh-KPDocID: 1r12d - View Document |
![]() | emea_strap_url_cmyk_rev_en_std_cent.eps MASTERDocID: 1qVx6 - View Document |
![]() | COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 10 December 2008 SECVolume IDocID: 1qH6O - View Document |
![]() | CMDh IP meeting November 2015 eSubmission Karin Gröndahl Head of Registration and Information Management, MPA, SwedenDocID: 1qFf7 - View Document |