Robuta

https://www.tga.gov.au/resources/guidance/classifying-medical-devices-are-not-vitro-diagnostics-ivds
Guidance to help manufacturers of medical devices classify their devices correctly.
in vitro diagnosticsmedical devicesclassifyingivds
https://www.bsigroup.com/en-GB/insights-and-media/insights/brochures/bsi-medical-devices-and-ivds-capacity-and-lead-times/
This document provides insights into BSI Notified Body and UK Approved Body lead times for Medical Devices & IVDs across all our technology teams.
medical deviceslead timesbsiivdscapacity
https://www.sgs.com/en-kg/webinars/2025/02/countdown-to-self-testing-ivds-transitional-deadline-act-now
Join our webinar as we explore the critical transition from IVDD to IVDR for self-test IVD manufacturers, covering classification, regulatory requirements and...
act nowcountdownselftestingivds
https://www.bsigroup.com/en-MY/insights-and-media/media/webinars/ukca-for-medical-devices-and-ivds-are-you-ready/
Ensure your medical devices and IVDs are ready for UKCA marking. Learn new regulatory requirements.
are you readymedical devicesukcaivdsbsi
https://extranet.who.int/prequal/
medical productsivdsmedicinesvaccines
https://www.bsigroup.com/en-HK/insights-and-media/insights/brochures/ukca-for-medical-devices-and-ivds/
Explore the UKCA marking process for medical devices and in vitro diagnostics (IVDs), ensuring regulatory compliance and market access in the UK.
medical devicesukcaivdsbsi