Europe and US set to work together to reduce barriers and increase trade in medical products. Cooperation could reduce manufacturing costs and improve controls.
Europe and US set to work together to reduce barriers and increase trade in medical products. Cooperation could reduce manufacturing costs and improve controls.
Obelis invites you to its 4th ERPA Annual Congress on Regulations and Compliance for Cosmetics and EAAR Annual MDR Conference on October 28-29, 2019.
The European Commission called for the creation of expert panels to advise and support on new EU medical device and in-vitro device regulations.
European Commission announce first four notified body designations and first CE certificate awarded under Medical Device Regulation 2017/745/EU.
Medical Devices Coordination Group have issued guidance on the new role of the EU Responsible Person under EU medical device and in-vitro device regulations.
The European Commission have published a new Borderline and Classification manual to accompany new medical device and in-vitro device regulations.
Who is responsible for CE marking on products in the EU, the original equipment manufacturer or the original brand labeller? Both! Find out why with Obelis.
An implementation decision has been published listing the entities designated to operate the Unique Device Identification (UDI) system for EU medical devices.
Person Responsible for Regulatory Compliance: unveiling its meaning and role under the MDR.
Global Medical Device Nomenclature agency have announced basic membership as a free service to all users. Find out how to join and how it works.