Staying up-to-date with Use-Lab

Use-Lab GmbH Successfully Passes ISO 9001 Audit Once Again

We are pleased to announce that Use-Lab GmbH has once again successfully passed the external ISO 9001 audit this year. This achievement reaffirms our ongoing commitment to quality, transparency, and continuous improvement across all areas of our company. ISO 9001 is the world’s most recognized standard for quality management systems, focusing on customer-oriented processes, efficient […]

HFES Symposium in Toronto, Canada March 30 – April 02, 2025

The HFES Symposium offers insights into the latest scientific findings, best practices and innovations in the field of patient safety in healthcare.

Thank You for a Successful 2024 – Merry Christmas!

We wish you a peaceful Christmas season and relaxing holidays. We, too, will be taking a Christmas break from December 24, 2024, to January 1, 2025.

Usability Engineering for Medical Devices using Artificial Intelligence and Machine Learning Technology

A position paper titled “Usability Engineering for Medical Devices using Artificial Intelligence and Machine Learning Technology” is now available.

MEDICA 2024: Join Us at the World’s Leading Medical Trade Fair!

Meet Torsten Gruchmann at Medica

China’s Regulatory Landscape for Medical Devices: A LinkedIn Series

Our Linked series guides you step-by-step through the most important processes in the regulatory landscape for medical devices in China.

“Lemonade from Lemons: Utilizing MDR’s Requirements for Your Marketing Claims!”

Symposium on medical technology by NSF live in Hamburg, September 19

New MDCG Documents on Medical Device Regulation Released

The Medical Device Coordination Group (MDCG) has released new guidelines for implementing the Medical Device Regulation (MDR). These documents provide crucial guidance for manufacturers and authorities.