Resource Library for Medical Device Professionals

6 total results. Show all resources.

In this recorded webinar we cover the major changes that have been made and tell you what needs to be done before you seek recertification by your Notified Body.watch now

Webinar | 1 hour

In this recorded webinar we will tell you how to deal with the issue of transitioning to another Notified Body and/or how to evaluate your options in establishing a new relationship.watch now

Webinar | 1 hour

In this webinar, we outline the most important MDR changes you need to know.watch now

Webinar | 1 hour

Within the next few years, the regulatory landscape will change dramatically for IVD companies selling in Europe. IVDR 2017/745 will be an entirely new classification scheme for IVDS, and places far more emphasis on clinical data and risk management watch now

Webinar | 1 hour

Europe's new Medical Devices Regulation (MDR) adds to the complexity of complying with specific PMS and post-market clinical follow-up (PMCF) requirements. In this free webinar, we discuss new European PMS and PMCF requirements.watch now

Webinar | 1 hour live webinar

This free recorded webinar is about risk management for medical device companies according to EN ISO 14971:2012.watch now

Webinar | One hour