Delivering technical communications to meet compliance and improve product adoption. Documentation, training, & cyber security. ISO 13485, EU MDR, MDSAP, more.
Big news: Novatek has merged with InfoPros! Our combined experience offers you new capabilities and extended resources to better support your needs, both now and in the future! Check out the press release on our blog. https://t.co/OUzP92zrul
IVDR regulation changes are on the horizon. Have you started planning? Read our blog for answers to the top 5 FAQs. https://t.co/Kn0nVG1E8Z
#IVDR#eumdr#mdr#regulatory#compliance
Congratulations to all those nominated for a #MEDTECH2019 Achievement Award. We’re honored to be among you! See the list of nominees: https://t.co/l1wmE4E41S
The new In-Vitro Device Regulations (IVDR 2017/746) being implemented in May 2022 are set forth to increase patient safety. In our latest blog we address some of the most common questions being asked regarding IVDR. https://t.co/N5ALSdikrb