Видео ютуба по тегу Eu Medical Device Regulation

EU MDR Vigilance & Trend Reporting: A Deep Dive into CAPA and FSCA Decisions
EU MDR Vigilance & Trend Reporting: A Deep Dive into CAPA and FSCA Decisions
EU Medical Device Directive to MDR Transition | Clinical Research & Regulatory Training
EU Medical Device Directive to MDR Transition | Clinical Research & Regulatory Training
Clinical Research Updates 2025: New European Regulation (CTIS) and ICH E6(R3)
Clinical Research Updates 2025: New European Regulation (CTIS) and ICH E6(R3)
EU MDR Clinical Evidence: Mastering CERs, PMCF, and Equivalence Arguments
EU MDR Clinical Evidence: Mastering CERs, PMCF, and Equivalence Arguments
Distributor in EU MDR | Article 14 Obligations & Practical Compliance Steps | Dr. Ashish Jha
Distributor in EU MDR | Article 14 Obligations & Practical Compliance Steps | Dr. Ashish Jha
EU Supply Chain Alert: Navigating Medical Device Shortage Notifications Under Regulation 2024/1860
EU Supply Chain Alert: Navigating Medical Device Shortage Notifications Under Regulation 2024/1860
EU IVDR Extension: Key Conditions & Deadlines Under Regulation 2024/1860
EU IVDR Extension: Key Conditions & Deadlines Under Regulation 2024/1860
Клинические требования к программному обеспечению как медицинскому изделию в соответствии с Регла...
Клинические требования к программному обеспечению как медицинскому изделию в соответствии с Регла...
ERN eUROGEN Webinar 138: Medical Device Shortages and Regulatory Constraints: An ERN Collaboration
ERN eUROGEN Webinar 138: Medical Device Shortages and Regulatory Constraints: An ERN Collaboration
Verordnung 🇪🇺 über Medizinprodukte ⚕️ (EU) 2017/745 (Medical Device Regulation, MDR)
Verordnung 🇪🇺 über Medizinprodukte ⚕️ (EU) 2017/745 (Medical Device Regulation, MDR)
Medical Devices in the Age of AI and Cybersecurity: Regulatory Insights | Compliance & Risks
Medical Devices in the Age of AI and Cybersecurity: Regulatory Insights | Compliance & Risks
Nelson Advisors predicts Distressed M&A's role in European HealthTech and MedTech in 2026
Nelson Advisors predicts Distressed M&A's role in European HealthTech and MedTech in 2026
Глава 5 | Часть 9 | Импорт исследуемых медицинских изделий | Форма MD-18 | L-18 | CDSCO MDR 2017
Глава 5 | Часть 9 | Импорт исследуемых медицинских изделий | Форма MD-18 | L-18 | CDSCO MDR 2017
EU MDR Clinical Investigations: Navigating Deadlines and Data Requirements for European Market Ac...
EU MDR Clinical Investigations: Navigating Deadlines and Data Requirements for European Market Ac...
An Introduction to the EU MDR 2017/745 Training Course
An Introduction to the EU MDR 2017/745 Training Course
EU's AI MedTech Ambush: Pure Global on the New RWE Mandate
EU's AI MedTech Ambush: Pure Global on the New RWE Mandate
MDD vs MDR: How Directive 93/42/EEC Was Replaced and What Manufacturers Must Do | Dr. Ashish Jha
MDD vs MDR: How Directive 93/42/EEC Was Replaced and What Manufacturers Must Do | Dr. Ashish Jha
Nelson Advisors European HealthTech and MedTech Market Shifts
Nelson Advisors European HealthTech and MedTech Market Shifts
Navigating AI in medical devices & healthcare – from hype to harmonization!
Navigating AI in medical devices & healthcare – from hype to harmonization!
Medical Device Regulatory Services Explained | FDA • EU • UK • ISO 13485
Medical Device Regulatory Services Explained | FDA • EU • UK • ISO 13485