by Innovit Corporate Affairs | May 28, 2021 | Ashley Howell, Blog, MDR, News
After four years of transition followed by a global pandemic in 2020, we reached a regulatory milestone on May 26, 2021 for Medical Device manufacturers in the European Union – with Medical Device Regulation 2017/745 finally taking effect. Yesterday, being the...
by Innovit Corporate Affairs | May 10, 2021 | Ashley Howell, Blog, Industry News
Today, medical device manufacturers are facing a wide array of data compliance demands from healthcare providers, and national regulators including the European Commission, FDA and China’s NMPA. With the introduction of GUDID and now EUDAMED, these repositories...
