In 2017, the European Union set a three-year transition period from your company’s current system of Active Implantable Medical Devices Directive (AIMDD) and the Medical Devices Directive (MDD) to the European Union Medical Device Regulation (EU MDR) and In Vitro Diagnostic Regulation (IVDR) regulations system. Even though the deadline to comply has been pushed to May 26, 2021 due to COVID-19, there is no reason to delay compliance! (NOTE: This webinar was recorded before the date was extended. Some deadlines will now be outdated; however, the reasons not to delay compliance remain the same.)
Watch this webinar on demand to learn how your organization can achieve European Union Medical Device Regulation (EU MDR) and In Vitro Diagnostic Regulation (IVDR) compliance. Learn what pitfalls to avoid to minimize disruption to business processes and ways to help your company transition smoothly and comply with the new regulations.
Ready to learn more?
Fill in to Download!
* fields are mandatory