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Published on:29 August 2025
Update
ATEX product directive conformity process
Uncategorized
Published on:4 September 2025
Update
The new EU Packaging Regulation: What medical device manufacturers need to know
Medical Devices
Published on:28 August 2025
Update
NIS2: What It Means and Who It Applies To
Uncategorized
Published on:27 August 2025
Update
Process Safety: A Must for Compliance with the Pressure Equipment Directive (PED) Assemblies
Uncategorized
Published on:31 July 2025
Update
The EU Toy Safety Regulation Is Coming: What Manufacturers Must Prepare For
Uncategorized
Published on:12 June 2025
Update
Become an expert in Quality Management with the Quality Manager (ISO 13485) training from Kader
General
Published on:16 May 2025
Update
Unlocking MedTech Innovation in Europe: A Call for Smarter, Faster Certification
Uncategorized
Published on:15 May 2025
Update
Strengthen Your Position in the Supply Chain with Demonstrable NIS2 Compliance
Uncategorized
Published on:10 April 2025
Update
Are you ready for the upcoming UDI deadline?
Uncategorized
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