November 20, 2018 - November 20, 2018
Date: 20 November 2018
Location: Radisson Blu Royal Hotel, Brussels, Belgium
Title: Addressing the Impact of the EU Medical Device Regulation (MDR) on ‘Combination’ Products
Gert Bos, Executive Director & Partner at Qserve Group is invited as speaker and presenter at the Inter-Regulatory and Stakeholder Workshop 2018.
TOPRA and RAPS, the leading organizations focused on supporting regulatory affairs professionals working in the healthcare sector, are collaborating to facilitate this inter-regulatory and stakeholder workshop to address changes introduced by the EU Medical Device Regulation (MDR) for device-drug and drug-device ‘combination’ product authorization. This workshop will bring together representatives of the European Commission, Member State medicinal, and medical device authorities, notified bodies and industry to discuss ambiguous areas to uncover practical implementation solutions that address the implications of the new requirements.
Visit the original website for more information and registration.