On-demand ICH GCP E6 (R3) training course
The International Council for Harmonisation (ICH) adopted the final version of Good Clinical...
Category: News
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...
New EQA schemes for 2025
We launch 5-10 new external quality assessment schemes annually. We closely monitor diagnostic...
EQA Program 2025
We proudly present the new external quality assessment program for 2025. The program includes over...
Does your device require a clinical investigation?
Are you developing a product intended to diagnose, treat, or prevent medical conditions? If so,...