Видео ютуба по тегу European Medical Devices Regulation

Understanding Compliance - U.S. FDA and EU MDR
Understanding Compliance - U.S. FDA and EU MDR
Mastering UK Medical Device Regulations UKCA Navigation & Compliance Post Brexit
Mastering UK Medical Device Regulations UKCA Navigation & Compliance Post Brexit
Is my product a Medical Device in Europe ? (EU MDR 2017/745)
Is my product a Medical Device in Europe ? (EU MDR 2017/745)
Europe's Emerging Medical Device Regulations (MDR) and Impacts on Medical Device Packaging
Europe's Emerging Medical Device Regulations (MDR) and Impacts on Medical Device Packaging
Clinical Evaluation Plan Template - Produce EU MDR-compliant CEPs for any class of medical device
Clinical Evaluation Plan Template - Produce EU MDR-compliant CEPs for any class of medical device
Beijing's tussle with Brussels: China retaliates on EU medical devices
Beijing's tussle with Brussels: China retaliates on EU medical devices
Spotlights: How AI is revolutionizing health care access? & Medical devices regulation | POLITICO
Spotlights: How AI is revolutionizing health care access? & Medical devices regulation | POLITICO
TOPRA Webinar - How to Optimize the Literature Review for Medical Devices for EU MDR Compliance
TOPRA Webinar - How to Optimize the Literature Review for Medical Devices for EU MDR Compliance
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Course
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Course
Want to get your medical device approved in Europe?
Want to get your medical device approved in Europe?
Medical devices regulation consultancy - MDR Regulator
Medical devices regulation consultancy - MDR Regulator
Podcast Episode – Simplifying EU Medical Device Regulations: The 2025 Proposal Explained
Podcast Episode – Simplifying EU Medical Device Regulations: The 2025 Proposal Explained
What are MDR 2017/745 compliance requirements sections for Medical Device Technical File
What are MDR 2017/745 compliance requirements sections for Medical Device Technical File
Rudi Tielemans - What does the new EU Medical Device Regulation mean to health software?
Rudi Tielemans - What does the new EU Medical Device Regulation mean to health software?
Global Registrations – Synergies Between US and Europe Medical Device Registration
Global Registrations – Synergies Between US and Europe Medical Device Registration
Extension of EU MDR Transition Timelines – Impact on Manufacturers
Extension of EU MDR Transition Timelines – Impact on Manufacturers
EU-MDR Clinical Evaluation of Software as a Medical Device (SAMD): Bringing it back to basics
EU-MDR Clinical Evaluation of Software as a Medical Device (SAMD): Bringing it back to basics
EU MDR extension for existing MDD certified medical devices Regulation (EU) 2023/60
EU MDR extension for existing MDD certified medical devices Regulation (EU) 2023/60
FIMEA designate first Notified Body under the IVD regulation in Finland
FIMEA designate first Notified Body under the IVD regulation in Finland
Medical Device Regulatory in Asia_Hong Kong
Medical Device Regulatory in Asia_Hong Kong
How to sell Medical Devices Online ? [EU and FDA]
How to sell Medical Devices Online ? [EU and FDA]
EU Postmarket Surveillance Requirements for Medical Devices
EU Postmarket Surveillance Requirements for Medical Devices
Reclassification of Medical Devices, upcoming revisions of EU regulations
Reclassification of Medical Devices, upcoming revisions of EU regulations
EU MDR – Regulation (EU) 2017/745 - Пошаговое руководство по соблюдению положений регламента*
EU MDR – Regulation (EU) 2017/745 - Пошаговое руководство по соблюдению положений регламента*
Integrating EU AI Act with MDR
Integrating EU AI Act with MDR