The UK giving new UK regulations to be applied to medical device manufacturers wishing to place their products on the UK Market after January 1st 2021.

The UK giving new UK regulations to be applied to medical device manufacturers wishing to place their products on the UK Market after January 1st 2021.
Expert guidance on the compliance process for the processing of personal data in the European Union according to the GDPR Regulation. Learn more here.
Obelis Academy, in collaboration with Norway Health Tech, present a series of Regulatory Breakfasts.
Along these courses, the experts will be addressing the most important topics to be prepared to meet the MDR deadline, with the possibility to book one-on-one meetings with the industry leaders to discuss your specific questions.
Due the 1-year delay will provide you with additional time to finalize your compliance with the MDR, but this is a complex and lengthy process!
As a matter of fact, we are only 9 months away from the date of application, while the full update to the MDR will take up to 18 months.
Let our experts guide you through the steps you need to follow to meet all the requirements in our webinar.
Due to the outbreak of the Covid-19 in Europe, the European Union is registering increasing shortages of test kits and IVD-related devices. IVD manufacturers need to move fast to secure the supply of such devices on the European market.
Join our FREE Webinar to find out how to register IVDs in Europe.
Remember, the 1-year delay will provide you with additional time to finalize your compliance with the MDR, which is a complex and lengthy process!
Due to the outbreak of the COVID-19 in Europe, the European Union was registering increasing shortages of Face Masks and other PPE-related equipment; PPE manufacturers needed to move fast to secure the supply of such equipment on the European market.
TEAM-PRRC Webinar, powered by TEAM-PRRC.
Medical device manufacturers are using these technologies to innovate their products to better assist healthcare providers and improve patient care.
Read more about seminars on Medical Device Regulations in the European Market.