Webinar – What you need to know to get your medical device approved

 In Event

Date: 18 June 2020 – 04PM CEST/10AM EDT

Place: Virtual

Replay: here

How the new Medical Device Regulation (MDR) will impact my business? What are the most important deadlines? How different will be the way to obtain the CE Mark? Which new requirements do I have to take into consideration?

These are certainly the recurrent questions you have been asking yourself for the past 3 years if you are a Medical Device Developer/Manufacturer, a CRO, a R&D center, or simply work in a MedTech-related area.

This webinar will help you to understand what steps need to be taken to bridge the gap between the current legislation and the new MDR compliance and anticipate many of the complexities of MDR implementation. You will learn in one hour the main MDR changes you should be aware of to get your product successfully certified.

DDR and Pharmaxi will tackle the impending MDR transition, focusing on main regulatory aspects to consider during your Medical Device development. Don’t wait until the end to make sure to be MDR-compliant and start planning your new regulatory strategy today!



About DDR: Drug Development and Regulation (DDR) is an independent European consultancy company, focused in providing appropriate scientific & regulatory expertise for the global development and registration of Drugs and Medical Devices.

Our valuable and tailor-made solutions contribute to the success of your development programs from a quality, nonclinical, clinical, and regulatory point of view.

Advantageously located in Barcelona, Amsterdam & London, DDR also benefits from a large network of highly qualified experts and strategic collaborations with renowned institutions worldwide.


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