medicaldeviceslegal

• About Erik Vollebregt
• EU Medical Devices Links

Category: MDR

• Erik Vollebregt

  

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• Medicaldeviceslegal tweets

  • EU #MDR date of application move: politically a done deal now #medicaldevices #medtech #eumdr… twitter.com/i/web/status/1… 1 month ago
  • New #MDCG guidance on temporary extraordinary measures related to medical device #NotifiedBody #audits during… twitter.com/i/web/status/1… 1 month ago
  • #MDR amendment proposal article 120 (3) oversight set to be fixed #medicaldevices #postponement #medtech #EUMDR… twitter.com/i/web/status/1… 1 month ago
  • The #MDR amendment proposal to move date of application by a year: more than meets the eye #medicaldevices #medtech… twitter.com/i/web/status/1… 1 month ago
  • Commission working on proposal to postpone #MDR date of application for one year #medicaldevices #medtech #eumdr medicaldeviceslegal.com/?p=6801 2 months ago
  • The #MDCG guidance on significant changes - a significant change? #medicaldevices #eumdr #medtech #MDR #IVDR… twitter.com/i/web/status/1… 2 months ago
  • The #MDR and the #Covid-19 recommendation - a possible template for fixing the MDR and #IVDR bottleneck… twitter.com/i/web/status/1… 2 months ago
  • New #MDCG Class I Article 120 (3) and (4) #MDR guidance - nothing new but nice summary of requirements… twitter.com/i/web/status/1… 2 months ago
  • The #MDCG #cybersecurity guidance - a helpful rush job #medicaldevices #ehealth #mhealth #medtech #euMDR #MDR #IVDR… twitter.com/i/web/status/1… 2 months ago
  • The #MDCG MDR joint implementation plan for the #MDR (not the #IVDR) #medicaldevices #medtech #eumdr… twitter.com/i/web/status/1… 2 months ago

• Most used tags on this blog

  3D printing advertising apps authorised representative Blue Guide borderline Brexit BSi business compliance CE marking Clinical evaluation Clinical investigation clinical trials COCIR Council Cybersecurity Dalli data protection Date of Application DIA Euromeeting e-labeling eHealth EN 14155 enforcement ENVI Eucomed Eudamed FCPA FDA GDPR genetic testing GHTF HCP hospitals in vitro diagnostics ivd IVDR ivds labeling Liese M&A market surveillance MDD MDR MEDDEV medicinal products mhealth mobile medical apps notified bodies notified body patents personal data PMA PMS post marketing surveillance product liability quality system Recast reprocessing revision Roth-Behrendt scrutiny Security seminar software standalone software standards subcontractors telemedicine transition plan transparency trilogue UDI Unannounced audits vigilance

• Recent comments

  	The 1-year delay for… on MDR date of application move:…
  	Axon Lawyers –… on New MDCG guidance on temporary…
  	COVID-19 CLINICAL EV… on Commission working on proposal…

• Most used categories on this blog

  Accessories Advertising Borderline Brexit Business compliance CE marking Clinical evaluation Clinical investigation Data Protection e-commerce eHealth Eudamed FCPA In Vitro Diagnostics IVDR Labeling M&A MDR mHealth Notified Body Personal data Placing on the market PMS Product liability Quality system Recast Software Standards Uncategorized Vigilance

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