Medical Device News DECEMBER 2025 Regulatory Update
Medboard Europe UK Standard EasyIFU Rest of the World Argentina Canada Brazil: Podcast Podcast Nostalgia – Let’s review previous podcasts Social Media to follow The post Medical Device News DECEMBER 2025 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir
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Show Notes
Medboard
Europe
- 48% disruption in the EU – I hope you are all healthy: https://health.ec.europa.eu/document/download/13b2c812-b144-4489-af1f-e76af5bc97fd_en?filename=md_availability_study_presentation_2024.pdf
- Consultation: SCHEER asks you – Are Brain Stimulators for non-medical purpose dangerous: https://health.ec.europa.eu/consultations/scheer-public-consultation-preliminary-scientific-opinion-health-hazards-and-risks-associated-use_en
- Q&A Medicines used with Medical Devices – Revision 6 with new questions: https://www.ema.europa.eu/en/documents/regulatory-procedural-guideline/questions-answers-implementation-medical-devices-vitro-diagnostic-medical-devices-regulations-eu-2017-745-eu-2017-746_en.pdf
- EUDAMED is Mandatory – From 28 May 2026: https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202502371 – https://health.ec.europa.eu/latest-updates/eudamed-four-first-modules-will-be-mandatory-use-28-may-2026-2025-11-27_en
UK
- Better Call MHRA – But we don’t consult: https://www.gov.uk/guidance/medical-devices-get-regulatory-advice-from-the-mhra
Standard
- ISO 10993-1 mutation – Nothing is automatic anymore: https://www.youtube.com/watch?v=AkSZVNSz5a0
- ISO 18969 draft – Comments until 28-01-2026: https://www.youtube.com/watch?v=zCR9HlHJ5l0
EasyIFU
- Create your Labels with EasyIFU – UDI included: https://easyifu.com
Rest of the World
Argentina
- Argentina: Simplified application – Class I/A or Class II/B: https://www.argentina.gob.ar/noticias/anmat-establece-un-regimen-simplificado-para-la-habilitacion-de-establecimientos
Canada
- Canada: Modernization of the MDEL – Some changes: https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/establishment-licences/medical-devices-compliance-bulletin/consultation-modernizing-mdel-framework-phase-ii.html
- Canada: Medical Device License Application – Guidance on how to do it: https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/managing-applications-licenses.html
Brazil:
- Brazil: Digitalisation of Certificates – You can request that online now: https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2025/anvisa-lanca-nova-ferramenta-para-emitir-certificados-de-dispositivos-medicos
Podcast
Podcast Nostalgia – Let’s review previous podcasts
- Episode 363 – The journey of a CRO with Helene Quie: https://podcast.easymedicaldevice.com/363-2/
- Episode 364 – What is changing with the new ISO 10993-1 with Marina Daineko: https://podcast.easymedicaldevice.com/364-2/
- Episode 365 – How to become a Lead Auditor with Rob Packard: https://podcast.easymedicaldevice.com/365-2/
Social Media to follow
- Monir El Azzouzi Linkedin: https://linkedin.com/in/melazzouzi
- Twitter: https://twitter.com/elazzouzim
- Pinterest: https://www.pinterest.com/easymedicaldevice
- Instagram: https://www.instagram.com/easymedicaldevice
The post Medical Device News DECEMBER 2025 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir