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

  • Versatile 2026 Delivered to SaaS Customers; On-Premises Coming Soon!
  • Lawsuit Challenges DOJ Presidential Records Act Memo: Perspectives and Practical Recordkeeping Lessons
  • Zasio Senior Analyst Frank Fazzio Earns AIGP Certification
  • Zasio Staffers to Present at ARMA North Dakota Spring Seminar
  • Seamlessly Automated Record Management: Smart Strategies for System-Ready Retention Schedules
©2026 Zasio Enterprises, Inc. All rights reserved.