Connect with Aurevia
Aurevia brings together expertise across clinical research, quality assurance, and regulatory ...
Category: Academia
Streamline your clinical study application
Regulatory requirements are becoming increasingly complex, and managing submissions, amendments, ...
CCLs: Bridging science and practice
At Aurevia, we have experienced Clinical Country Liaisons (CCLs), a role that shares many ...
CTIS updates
The Clinical Trials Information System (CTIS) has introduced several updates aimed at improving ...
Prepare your clinical study for success
Many innovative therapies and medical technologies face the same challenge: you know a clinical ...
Recent clarification in Sweden’s clinical trial legislation
From 1 July 2026, a clarification in the Swedish Medicines Act has further defined the role of ...
Improved flexibility for CTIS submissions
A new “Article 11 workaround” is addressing a long-standing limitation in CTIS when working with ...
Clinical trial launched to improve outcomes in emergency surgery
We are excited to share that an investigator-initiated study, led by Erik Osterman and Fredrik ...
Investigator-initiated clinical trials
Many important clinical studies start with researchers – not pharmaceutical companies. In ...