We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
The European Union’s Medical Device Coordination Group released a trio of guidances that clarify devicemakers’ responsibilities for implementing unique device identification systems under the EU’s new Medical Device Regulations. Read More
Health Canada is sticking to its compliance deadline of Jan. 1, 2019, for devicemakers selling products in Canada to transition to the Medical Device Single Audit Program, but it is making adjustments to help manufacturers comply. Read More
Following consultation with stakeholders, India’s Drugs Controller General adopted essential principles for safety and performance of medical devices marketed in India. Read More
Following up on a proposal from Australia’s Therapeutic Goods Administration, the International Medical Device Regulators Forum released a new consultation on personalized medical devices following its March meeting in Shanghai. Read More