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EMA : Donner votre avis sur un document de réflexion concernant la gestion de la qualité dans les essais cliniques Imprimer
Nouvelles de l'EMA
The European Medicines Agency has recently released a draft reflection paper on risk based quality management in clinical trials.

The purpose of this reflection paper is to facilitate the development of a more systematic, prioritised, risk-based approach to quality management of clinical trials, to support the principles of Good Clinical Practice and to complement existing quality practices, requirements and standards.

The document is available for consultation by clicking here

Comments related to this reflection paper should be provided using this template. The completed comments form should be sent to Cette adresse email est protégée contre les robots des spammeurs, vous devez activer Javascript pour la voir. .

Please note that the deadline for comments for this reflection paper is 15 February 2012.

We would be grateful if you could disseminate this email to anyone else who might be interested in this document.
With kind regards,

Alessandro Camera | Medical Information Sector
European Medicines Agency | 7 Westferry Circus | Canary Wharf | London E14 4HB | United Kingdom
Tel. +44 (0)20 7418 8724 | Fax +44 (0)20 7523 7129 | Cette adresse email est protégée contre les robots des spammeurs, vous devez activer Javascript pour la voir. | www.ema.europa.eu

 
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