Archive: European Medicines Agency

Showing 491 to 500 of 575 entries

	Title
2008-06-01	EMEA implementation of electronic-only submission and e-CTD submission: Questions and answers relating to practical and technical aspects of the implementation Author (Corporate): European Medicines Agency Published: June 2008 (Last update: 01/06/2008)
2008-05-01	Annual report of the European Medicines Agency 2007 Author (Corporate): European Medicines Agency Published: May 2008 (Last update: 01/05/2008)
2008-04-23	Reflection paper on benefit-risk assessment methods in the context of the evaluation of marketing authorisation applications of medicinal products for human use Author (Corporate): European Medicines Agency Published: 23/04/2008 (Last update: 23/04/2008)
2008-04-08	Work programme for the European Medicines Agency 2008 Author (Corporate): European Medicines Agency Published: 08/04/2008 (Last update: 08/04/2008)
2008-03-10	Press Release: EMEA reports strong performance in regulatory and public-health activities in 2007; the outlook for 2008 is even higher application numbers and a focus on advanced-therapy medicines Author (Corporate): European Medicines Agency Series Details: Press Release EMEA/MB/117248/2008 (10.3.08) Published: 10/03/2008 (Last update: 10/03/2008)
2008-03-01	Survey 2007 on the performance of EMEA scientific procedures for medical products for human use Author (Corporate): European Medicines Agency Published: March 2008 (Last update: 01/03/2008)
2008-02-21	Press Release: EMEA recommends authorisation of first pre-pandemic influenza vaccine Author (Corporate): European Medicines Agency Series Details: Press Release EMEA/CHMP/90694/2008 (21.2.08) Published: 21/02/2008 (Last update: 21/02/2008)
2008-02-01	Ethical considerations for clinical trials on medicinal products conducted with the paediatric population: Recommendations of the ad hoc group for the development of implementing guidelines for Directive 2001/20/EC relating to good clinical practice in the conduct of clinical trials on medicinal products for human use Author (Corporate): European Medicines Agency Published: February 2008 (Last update: 01/02/2008)
2008-01-22	EMEA implementation of electronic-only submissions and e-CTD submissions in the centralised procedure: Statement of intent Author (Corporate): European Medicines Agency Published: 22/01/2008 (Last update: 22/01/2008)
2008-01-01	Report on the progress of the interaction with patients’ and consumers’ organisations and analysis of the degree of satisfaction of patients/consumers involved in EMEA activities during 2007 Author (Corporate): European Medicines Agency Published: 2008 (Last update: 01/01/2008)