medicaldeviceslegal

Medical devices legal and regulatory blog

  • About Erik Vollebregt
  • EU Medical Devices Links

Tag browsing: CE marking

The new Blue Guide is here

CE certification of standalone software and apps seminar – the movie

CE marking of apps: It Can Be Done and Here Is How

Outlines of the medical devices Recast become more fixed with Council conclusions

Improving implementation: the Code for Notified Bodies

M&A seminar: EU legal & regulatory aspects

New standard for medical technology used at home

« Older posts

  • 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

  • Enter your email address to subscribe to this blog and receive notifications of new posts by email.

    Join 4,517 other followers

  • Subscribe via RSS

    RSS Feed RSS - Posts

    RSS Feed RSS - Comments

  • All content on this blog is subject to a Creative Commons Licence

  • 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

Blog at WordPress.com.

medicaldeviceslegal
Blog at WordPress.com.
Cancel