Check out our IVDR transition FAQ on Regulation (EU) 2024/1860. Stay tuned on BSI In Vitro Diagnostics Regulatory Services for upcoming guidance!
Check out our IVDR transition FAQ on Regulation (EU) 2024/1860. Stay tuned on our dedicated IVDR webpage for upcoming guidance: https://bit.ly/3xUn9Ow #BSI #MedicalDevices #IVDR #AmendingRegulation
Check out our IVDR transition FAQ on Regulation (EU) 2024/1860. Stay tuned on our dedicated IVDR webpage for upcoming guidance: https://bit.ly/3xUn9Ow #BSI #MedicalDevices #IVDR #AmendingRegulation
Check out our IVDR transition FAQ on Regulation (EU) 2024/1860. Stay tuned on our dedicated IVDR webpage for upcoming guidance: https://gag.gl/SYDweM #BSI #MedicalDevices #IVDR #AmendingRegulation
Business Development Manager @ BSI | Regulatory Services - Supporting IVD Manufacturers to Achieve Regulatory Compliance and Market Access.
Check out our IVDR transition FAQ on Regulation (EU) 2024/1860. Stay tuned on our dedicated IVDR webpage for upcoming guidance: https://gag.gl/SYDweM #BSI #MedicalDevices #IVDR #AmendingRegulation
Check out our IVDR transition FAQ on Regulation (EU) 2024/1860. Stay tuned on our dedicated IVDR webpage for upcoming guidance: https://gag.gl/SYDweM #BSI #MedicalDevices #IVDR #AmendingRegulation
Check out our IVDR transition FAQ on Regulation (EU) 2024/1860. Stay tuned on our dedicated IVDR webpage for upcoming guidance: https://gag.gl/SYDweM #BSI #MedicalDevices #IVDR #AmendingRegulation
Check out our IVDR Transition Guidance to discover key elements of Regulation (EU) 2024/1860 and to easily navigate the possible implications for your business and understand the conditions you are required to meet to continue placing IVDs on the EU market. Stay tuned on our IVDR dedicated webpage for upcoming guidance: https://gag.gl/La4Oup #BSI #MedicalDevices #IVDR #AmendingRegulation
Business Development Manager @ BSI | Regulatory Services - Supporting IVD Manufacturers to Achieve Regulatory Compliance and Market Access.
Check out our IVDR Transition Guidance to discover key elements of Regulation (EU) 2024/1860 and to easily navigate the possible implications for your business and understand the conditions you are required to meet to continue placing IVDs on the EU market. Stay tuned on our IVDR dedicated webpage for upcoming guidance: https://gag.gl/La4Oup #BSI #MedicalDevices #IVDR #AmendingRegulation
Check out our IVDR Transition Guidance to discover key elements of Regulation (EU) 2024/1860 and to easily navigate the possible implications for your business and understand the conditions you are required to meet to continue placing IVDs on the EU market. Stay tuned on our IVDR dedicated webpage for upcoming guidance: https://bit.ly/3zLhomy #BSI #MedicalDevices #IVDR #AmendingRegulation
Check out our IVDR Transition Guidance to discover key elements of Regulation (EU) 2024/1860 and to easily navigate the possible implications for your business and understand the conditions you are required to meet to continue placing IVDs on the EU market. Stay tuned on our IVDR dedicated webpage for upcoming guidance: https://gag.gl/La4Oup #BSI #MedicalDevices #IVDR #AmendingRegulation
Helping companies manage the requirements and traceability of complex mission and safety critical software systems
IVDR Delayed. It looks like there's going to be delay to the implementation of the IVDR rules and it could be for up to 31 months. Have a read of this short article by Medtechdive: https://lnkd.in/eehpA-WS
