medicaldeviceslegal

• About Erik Vollebregt
• EU Medical Devices Links

Tag browsing: DIA

• Erik Vollebregt

  

  Erik is a founding partner of the boutique life sciences law firm Axon Lawyers and specialised in EU legal and regulatory issues relating to medical technology

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• Medicaldeviceslegal tweets

  • Netherlands to adopt act on #medicaldevices hospitality and Sunshine reporting medicaldeviceslegal.com/2017/06/05/net… https://t.co/QwnWuqyJFf 2 weeks ago
  • #medicaldevices #IVDs #medtech twitter.com/meddevlegal/st… 1 month ago
  • RT @mstrubin: Glad to speak at #eHealthWeek on 10 May in the session "Nobody said it would be easy" on @EURO_CAS and #interoperability. @eH… 1 month ago
  • Final MDR and IVDR texts published medicaldeviceslegal.com/2017/05/05/fin… https://t.co/BV73UcRto5 1 month ago
  • Check out our session on #medicaldevices and #dataprotection compliance in global big data at 11:00 today at #GMTCC gmtcc.com/programme-2017 1 month ago
  • New EU #medicaldevices and #IVD regulations to be published this Friday medicaldeviceslegal.com/2017/05/03/mdr… https://t.co/y0jK0x4jqi 1 month ago
  • RT @EU_Growth: New rules for #MedicalDevices🌡️ adopted by @Europarl_EN for better patient protection and greater transparency: https://t.co… 2 months ago
  • EU SCHEER scientific advice on breast implants published, consultation until 7 May #medicaldevices #breastimplants ec.europa.eu/newsroom/sante… 2 months ago
  • EU Parliament vote final stage of adoption of new EU rules for #medicaldevices and #IVDs medicaldeviceslegal.com/2017/04/06/mdr… https://t.co/m6iiV5YrLW 2 months ago
  • This is it: EU #MDR & #IVDR texts final and ready for voting #medicaldevices #ivds medicaldeviceslegal.com/2017/03/05/thi… https://t.co/Kc0gOTVKau 3 months ago

• Most used tags on this blog

  3D printing advertising apps authorised representative borderline business compliance CE mark CE marking Clinical evaluation Clinical investigation clinical trials COCIR competition law conferences Council Cybersecurity Dalli data protection DIA 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 promotion quality system Recast reprocessing revision Roth-Behrendt scrutiny Security seminar software standards subcontractors telemedicine transition plan transparency trilogue UDI Unannounced audits vigilance

• Recent comments

  	Julie O. on Final MDR and IVDR texts …
  	Erik Vollebregt on Product liability for devices…
  	Rod Ruston on Product liability for devices…

• Most used categories on this blog

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

• Archives

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