The importance of a robust Design and Development (D&D) process in medical device companies
In the competitive and highly regulated world of medical technology, a robust and well-structured...
Here are the latest news from Aurevia. Keep track of what's happening!
In the competitive and highly regulated world of medical technology, a robust and well-structured...
The industry's financing climate has slowed down considerably. Investments in the development of...
The International Council for Harmonisation (ICH) adopted the final version of Good Clinical...
The Health Technology Assessment Regulation (HTAR), officially known as Regulation (EU) 2021/2282,...
Registration for Labquality Days 2026 is now open! Take advantage of the Super Saver prices by...
Navigating the regulatory landscape of the medical device sector is a complex task, requiring both...
Our international EQA team welcomes you to visit our exhibition booth number 13 at EuroMedLab,...
In January 2025, the Aurevia brand was established when Labquality, Artimed, Clinical Consulting,...
This year the European Society for Clinical Microbiology and Infectious Diseases, ESCMID Global,...
We are delighted to announce the appointment of the new Head of the EQA business area Jonna Pelanti...
Aurevia’s international EQA team welcomes you to visit our exhibition booth A18 at BioMedica, which...
We are delighted to announce the appointment of the new Head of the CRO business area Ulrika...