Developing a guide to regulations forthe Medical Device Industry
All Medical devices are required to go through regulatory processes before they can be put onthe market. The regulatory processes differ depending on what market is the aim. To releasemedical devices within the European Economic Area (EEA) the devices need to have a CEmarking affixed. To release wit...
| Main Authors: | , |
|---|---|
| Format: | Others |
| Language: | English |
| Published: |
KTH, Maskinkonstruktion (Inst.)
2014
|
| Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-146630 |