Zasio
  • Software
    • Retention Schedule Management
    • Electronic Records Management
    • Physical Records Management
  • Consulting
    • Services In Demand
    • Records Retention Schedule
    • Privacy
    • Information Governance 101
    • Meet Our Team
    • Virtual Coffee With Consulting
    • Request Assessment
  • News & Events
  • Industries
  • Information Security
  • Support
  • About
    • Careers
    • Contact
  • LOG IN
  • Request Info
Select Page
New Changes to the European Union’s Medical Device and In Vitro Diagnostic Device Regulations

New Changes to the European Union’s Medical Device and In Vitro Diagnostic Device Regulations

by Zasio | Oct 12, 2020 | Blog, By Heather Rice

On May 26, 2020, the European Union enacted new regulations concerning medical and in vitro diagnostic devices—a move that should cause manufacturers, clinical trial sponsors, investigators, and other regulated parties involved in medical device development,...

Recent Posts

  • Updating Your Retention Schedule Too Often Puts Your Organization at Risk
  • From Chatbot to Courtroom: AI Records in Litigation
  • Data Traceability in the Age of AI
  • Mexico Records Retention Requirements
  • Zasio Senior Analyst Michaela Adams Earns IGP Certification
©2026 Zasio Enterprises, Inc. All rights reserved.