PolarCool receives timeline for MDR certification
The med-tec company PolarCool AB (publ) announces that it has received a timeline from Intertek for approval of the company's own quality management system (QMS), under the EU's new Medical Device Regulation (MDR). In an ongoing process with the Notified Body (NB) Intertek, PolarCool has made important progress in obtaining approval for the company's own quality management system ISO 13485 within the new MDR regulations. Intertek has provided PolarCool with a timeline for the upcoming certification process, the first part of which will begin in this autumn. The final part, which is a