| Numéro | 111 |
|---|---|
| Titre | Medical device regulations: Global overview and guidind principles |
| Rubrique | Informations générales sur le don d'équipement |
| Auteur | OMS |
| Editeur | OMS |
| Résumé | The purpose of this publication is to provide guidance to Member States wishing to create or modify their own regulatory systems for medical devices. It is recognized that there is no single template that will respond to the needs of every country. Some countries may have production facilities that will require good manufacturing practice and complex quality controls; others may depend principally on the donation of equipment from externa sources and need different policies to protect their population against unsafe and inappropriate technology. Resources, both human and financial, remain a significant factor in the progressive development of national regulatory authorities. Nevertheless, there are many ways that governments can benefit from the wealth of experience of others, and start to build efficient medical device regulatory systems. This publication highlights the most important of these. |
| Prix | 0 |
| Lien site web | http://www.who.int/medical_devices/publications/en/MD_Regulations.pdf |
| Détail langue | |
| Lien de téléchargement | Télécharger le document |
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