International Medical Device Regulatory Monitor
July 2012
| Vol.
20 No.
7
Sweden Seeks Further Clarification on Stand-Alone Software as a Device
Sweden’s Medical Products Agency (MPA) is asking a European Commission working group to address certain issues before adopting a draft guideline on when a stand-alone software program is regulated as a medical device.
This article is viewable by subscribers only. To view this article, please select an option below.
|