ECM CE Marking for Medical Devices
  • Who We Are
    • About Us
    • Why ECM
    • Mission & Vision
    • Meet Our Key People
    • We Are Hiring
  • What We Do
    • Testing
    • CE Marking
      • MDR
    • ISO 13485
    • Transfers
    • Signature Services
      • Express Service
      • On Time Service
    • FDA
    • International Approvals
  • Library
    • Resources
    • White Papers
  • Contact
  • Blog
Select Page
Testing According to EN 60601

Testing According to EN 60601

by Federica Secchi | Aug 11, 2019 | White Papers

Notice: JavaScript is required for this...
Technical File – Technical Documentation and the MDR

Technical File – Technical Documentation and the MDR

by Federica Secchi | Jul 28, 2019 | White Papers

Notice: JavaScript is required for this...
Differences between ISO 9001:2015 and ISO 13485:2016

Differences between ISO 9001:2015 and ISO 13485:2016

by Federica Secchi | Jul 7, 2019 | White Papers

Notice: JavaScript is required for this...
The EU-MDR From a Notified Body Perspective

The EU-MDR From a Notified Body Perspective

by Federica Secchi | Jun 18, 2019 | White Papers

Notice: JavaScript is required for this...
Transitioning from the MDD to the New EU MDR

Transitioning from the MDD to the New EU MDR

by ecmamerica | Mar 29, 2019 | White Papers

Notice: JavaScript is required for this...
ECM Planning for Implementation of the EU MDR

ECM Planning for Implementation of the EU MDR

by ecmamerica | Mar 28, 2019 | White Papers

Notice: JavaScript is required for this...
  • Facebook
  • Twitter
ECM America | Copyright ® 2019 | Website Powered By Mello Multimedia