Executives & regulatory representatives of Medispec Ltd.
1 contact identified
SPECTOR Avner
Assuring the conformity of devices with the quality management system (QMS), ensuring that technical documentation and the EU documentation of conformity are generated and are up to date, ensuring that the company complies with post-market surveillance obligations listed in Article 10(10) of MDR and that the company fulfils its reporting obligations, found in Articles 87-91 of MDR.