Developing a guide to regulations forthe Medical Device Industry
All Medical devices are required to go through regulatory processes before they can be put on the market. The regulatory processes differ depending on what market is the aim. To release medical devices within the European Economic Area (EEA) the devices need to have a CE marking affixed. To release...
| Main Authors: | , |
|---|---|
| Format: | Others |
| Language: | English |
| Published: |
KTH, Industriell produktion
2014
|
| Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-142032 |