Blog
Filtering
Published on:30 January 2025
Update
Important Changes in the EU Product Liability Directive: What Does This Mean for Medical Devices?
Medical Devices
Published on:14 November 2024
Update
Navigating the New IGJ Guidance on Post-Market Surveillance
Uncategorized
Published on:22 October 2024
Update
Certification Experts Expands with New Office in Switzerland
Authorised Representation
Published on:3 October 2024
Update
The New Machinery Regulation
Machinery
Published on:26 July 2024
Update
Certification Experts Expands its Services with the Acquisition of CEpartner4U
General
Published on:19 April 2024
Update
Software as a Medical Device: smarter compliance with regulations
Medical Devices
Published on:2 April 2024
Update
Important Deadlines for EU MDR transition: Legacy Medical Devices to MDR Compliance
Medical Devices
Published on:6 March 2024
Update
Framework for Post-Market Surveillance (PMS)
Medical Devices
Published on:2 September 2019
Update
Who is responsible for the correct use of the CE mark?
CE Marking
Published on:23 March 2021
Update
Expert Insights: US/Canada Product Compliance
Canada
International
USA Compliance
Published on:28 November 2016
Update
NEN-EN 1090, 1 July 2014
Construction Products
Published on:28 November 2023
Update
The most efficient Risk Assessment with Safexpert
CE Marking
Electronics and Electrical equipment
Machinery