Argos Multilingual
2 min. read
Certified Language Service Providers for MDR Regulation Changes
While the earlier Medical Device Regulations referred specifically to ISO 9001, the new regulations no longer stipulate a compulsory ISO standard. That said, ISO 13485:2016 is generally recognized as the industry standard for Medical Devices in the EU, and, while a manufacturer’s certification body can provide more detailed advice, ISO 13485 is likely to be […]
