Many manufacturers of medical devices are certified according to EN ISO 13485 as basis for their management system for the development and production of medical devices. In order to adjust to the current EU-Directives (90/385/EEC, 93/42/EEC and 98/79/EC) for medical devices EN ISO 13485 will be revised.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |