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MDR Series: TIPS with ISA. Tip 2: Addressing the EU MDR Date of application Inconsistency. With EU MDR delayed one year, where is the industry at today? How can you navigate this recent extension? Watch now to learn

Join us as MedEnvoy's Regulatory Affairs Consultant Emma Knijn discusses the unique challenges faced by Software as a How does it work? We analyze customer current situation; we identify opportunities for improving the processes in all the company

An Overview of the EU Medical Device Regulation MDR and In Vitro Diagnostics Regulation IVDR PREVIEW Navigating MDR and IVDR compliance can be complex, but we've got you covered! In this webinar with Notified Body expert,