20 Dec, 2022 Health Software, Regulatory Affairs, Regulatory Affairs MedTech standards and regulations for artificial intelligence by Hinsija Schilling
21 Oct, 2022 Regulatory Affairs Testing for cytotoxicity: The “well-established” EN ISO 10993-5 by Alexandra Grosu
17 Aug, 2022 Regulatory Affairs Electronic instructions for use – The hidden duty of MDR by seleonadmin
02 Aug, 2022 Health Software, Regulatory Affairs Artificial Intelligence Basics for medical technology by seleonadmin
26 Jul, 2022 Lifecycle Processes, Regulatory Affairs Caution, distributor! Or manufacturer after all …? by seleon
04 Jul, 2022 Regulatory Affairs Tests for irritation: The EN ISO 10993-23 extends the series of standards by seleonadmin
25 May, 2022 Lifecycle Processes, Regulatory Affairs Riding the wave means being successful by seleon
30 Sep, 2021 Clinical Affairs, Health Software, Lifecycle Processes, Regulatory Affairs The Way out of the MDR standards jungle by seleon