The Swedish Medical Products Agency (Läkemedelsverket) is offering a webinar for those who work with the development of in vitro diagnostic medical devices (IVDs). The webinar will provide an overview of regulatory processes included in the IVD Regulation (IVDR) such as submitting an application for an IVD clinical performance study.
Don’t miss out on this opportunity to learn more about the regulatory requirements overseeing the IVD medical device product lifecycle.
Join this webinar (in Swedish) on November 16th – Register now
Learn more about IVD development:
Good study practice for IVDs – ISO 20916
5 questions about medical devices
At Scandinavian CRO, we have the medical device expertise to help you with all aspects of your clinical investigations from planning, designing, and executing through to analysis and reporting. Contact us
