Видео ютуба по тегу European Medical Devices Regulation

EU MDR & IVDR 2025 Reforms: What They Mean for Diagnostics, Pharma, and Companion Diagnostics
EU MDR & IVDR 2025 Reforms: What They Mean for Diagnostics, Pharma, and Companion Diagnostics
Nelson Advisors 2026 Cryogenics Wellness Revolution
Nelson Advisors 2026 Cryogenics Wellness Revolution
Medical Device Regulatory Services Explained | FDA • EU • UK • ISO 13485
Medical Device Regulatory Services Explained | FDA • EU • UK • ISO 13485
Strategies for Navigating the EU MDR Extension Deadlines
Strategies for Navigating the EU MDR Extension Deadlines
How to Run a Device Performance Study under EU MDR — Annex XV & Practical Steps | Dr. Ashish Jha
How to Run a Device Performance Study under EU MDR — Annex XV & Practical Steps | Dr. Ashish Jha
Война между ЕС и Китаем в сфере медицинских изделий привела к резкому росту торговых запретов и п...
Война между ЕС и Китаем в сфере медицинских изделий привела к резкому росту торговых запретов и п...
Podcast Episode – Simplifying EU Medical Device Regulations: The 2025 Proposal Explained
Podcast Episode – Simplifying EU Medical Device Regulations: The 2025 Proposal Explained
RAPS Euro Convergence 2026 is the most comprehensive regulatory affairs conference in Europe
RAPS Euro Convergence 2026 is the most comprehensive regulatory affairs conference in Europe
Pure Global: KSA's EU MDR Bridge & The Hidden Regulatory Traps
Pure Global: KSA's EU MDR Bridge & The Hidden Regulatory Traps
Custom-Made Medical Devices (EU MDR) | Definition, Annex XIII & Manufacturer Duties | Dr. Ashish Jha
Custom-Made Medical Devices (EU MDR) | Definition, Annex XIII & Manufacturer Duties | Dr. Ashish Jha
EU MDR and IVDR Proposal for Reboot (December 2025)
EU MDR and IVDR Proposal for Reboot (December 2025)
Global Regulatory Updates from the US, EU, Brazil, and Turkey
Global Regulatory Updates from the US, EU, Brazil, and Turkey
Medical Device Labeling Importer & Rep Requirements Explained
Medical Device Labeling Importer & Rep Requirements Explained
MedTech Compliance Simplified. Master MDR & EU AI Act implementation.
MedTech Compliance Simplified. Master MDR & EU AI Act implementation.
EU Health Breakthroughs 2025: Biotech Act, Safe Hearts, and Faster Medical Devices
EU Health Breakthroughs 2025: Biotech Act, Safe Hearts, and Faster Medical Devices
US FDA Medical Device Regulation
US FDA Medical Device Regulation
📊 48% Disruption in the EU Medical Device Market — Are You Ready?
📊 48% Disruption in the EU Medical Device Market — Are You Ready?
Europe's New Cyber Rules: Pure Global on MedTech's Security Hurdles
Europe's New Cyber Rules: Pure Global on MedTech's Security Hurdles
Conformity Assessment in EU MDR | Annex IX, X, XI Explained | Dr. Ashish Jha
Conformity Assessment in EU MDR | Annex IX, X, XI Explained | Dr. Ashish Jha
Medical Device News DECEMBER 2025 Regulatory Update-What You Need to Know
Medical Device News DECEMBER 2025 Regulatory Update-What You Need to Know
Webinar: From USA to Europe - Accelerating Your Path to the Medical Device Market
Webinar: From USA to Europe - Accelerating Your Path to the Medical Device Market
Breakthrough Device Designation in the EU: A New Regulatory & Market Access Pathway
Breakthrough Device Designation in the EU: A New Regulatory & Market Access Pathway
Global Regulatory Updates from India, Guatemala, Egypt, and EU
Global Regulatory Updates from India, Guatemala, Egypt, and EU
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
График перехода к регулированию медицинских изделий в ЕС
График перехода к регулированию медицинских изделий в ЕС