medicaldeviceslegal

• About Erik Vollebregt
• EU Medical Devices Links

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• 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

  • "Rising healthcare costs not directly tied to medical technology, according to study" #medicaldevices massdevice.com/blogs/massdevi… 1 day ago
  • EU moving forward with discussions on revision of #Batteries Directive, relevant also for #medicaldevices consilium.europa.eu/uedocs/cms_Dat… 1 day ago
  • “Convenient guide for Dutch #medtech starters "De wereld van de Medtech starter" medicaldevices #eu_mdd” hollandhealthtech.nl/site/archives/… 2 days ago
  • RT @RobertMDProject: Erik's blog on cybersecurity. Want help to build your technical file? mdproject.nl medicaldeviceslegal.com/2013/06/17/fda… 2 days ago
  • Convenient comprehensive guide for NL #medtech starters "De wereld van de Medtech starter" powered by @AxonLawyers #medicaldevices #eu_mdd 2 days ago
  • FDA's draft guidance on #cybersecurity for #medicaldevices: nothing exciting but useful examples wp.me/p1btIG-oQ 2 days ago
  • Interesting perspective on patient centered care: "If You’re Not Patient-Centered, Walmart Will Be" #hospitals community.advanceweb.com/blogs/xi_1/arc… 5 days ago
  • "@Eucomed / @medtecheurope guidance clarifies RoHS compliance for medical device companies" #medicaldevices massdevice.com/blogs/arezu-sa… 6 days ago
  • "FDA wants tighter cybersecurity for medical devices - Fierce #MedicalDevices" #medtech #eu_mdd fiercemedicaldevices.com/story/fda-want… 6 days ago
  • "The Tangled Destinies of Europe’s #UDI, #Eudamed Database and #MedicalDevices Regulation" #medtech #eu_mdd medtechinsider.com/archives/31380 6 days ago

• Most used tags on this blog

  advertising apps borderline business compliance CE marking Clinical evaluation Clinical investigation Dalli data protection DIA Euromeeting e-labeling eHealth EN 14155 ENVI Eucomed Eudamed FCPA FDA GHTF in vitro diagnostics ivd ivds labeling Liese M&A MDD MEDDEV mhealth mobile medical apps notified bodies notified body patents PMA PMS post marketing surveillance product liability quality system Recast revision Roth-Behrendt seminar software standards subcontractors telemedicine

• Recent comments

  	FDA’s draft gu… on eHealth and mHealth at the DIA…
  	FDA’s draft gu… on EU privacy requirements for (h…
  	FDA’s draft gu… on Team NB FAQ on EN62304 standar…

• Most used categories on this blog

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

• Archives

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