New EQA Pilot Studies 2025
At Aurevia, we actively follow the development of laboratory medicine as we want to produce...
Category: News
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...
Tough times require sharp strategies – and the right expertise
The industry's financing climate has slowed down considerably. Investments in the development of...
On-demand ICH GCP E6 (R3) training course
The International Council for Harmonisation (ICH) adopted the final version of Good Clinical...
Does the Health Technology Assessment Regulation (HTAR) include medical devices?
The Health Technology Assessment Regulation (HTAR), officially known as Regulation (EU) 2021/2282,...
Registration for Labquality Days 2026 is open!
Registration for Labquality Days 2026 is now open! Take advantage of the Super Saver prices by...
Regulatory strategy vs. regulatory intelligence
Navigating the regulatory landscape of the medical device sector is a complex task, requiring both...
Meet us at EuroMedLab in Brussels!
Our international EQA team welcomes you to visit our exhibition booth number 13 at EuroMedLab,...
Meet us at ESCMID 2025 in Vienna
This year the European Society for Clinical Microbiology and Infectious Diseases, ESCMID Global,...
Meet us at BioMedica in Dublin
Aurevia’s international EQA team welcomes you to visit our exhibition booth A18 at BioMedica, which...
Introducing the EQA Pilot Studies 2025
At Aurevia, we actively follow the development of laboratory medicine as we want to produce...
Introducing Aurevia
On January 7th, Labquality and Artimed, Clinical Consulting, Kasve and Prisma CRO merge under the...