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,...
QAdvis and Scandinavian CRO join Aurevia to strengthen clinical research and regulatory expertise
In January 2025, the Aurevia brand was established when Labquality, Artimed, Clinical Consulting,...
Meet us at ESCMID 2025 in Vienna
This year the European Society for Clinical Microbiology and Infectious Diseases, ESCMID Global,...
Aurevia appoints Jonna Pelanti as the new Head of EQA business area
We are delighted to announce the appointment of the new Head of the EQA business area Jonna Pelanti...
Meet us at BioMedica in Dublin
Aurevia’s international EQA team welcomes you to visit our exhibition booth A18 at BioMedica, which...
Aurevia appoints Ulrika Hammarström as the new Head of CRO business area
We are delighted to announce the appointment of the new Head of the CRO business area Ulrika...