Clinical Trial Services: Order Services From Aurevia AB

Aurevia AB says researchers can now order services to support clinical drug trials, medical device investigations, and other clinical studies. The consulting company offers assistance with Clinical Trial Information System (CTIS) applications, protocol writing, monitoring, and project management. Among the listed options are preparation and submission of clinical trial applications and Substantial Modification applications in CTIS, preparation of Annual Safety Reports, and reporting clinical trial results after study completion. Aurevia AB also supports device and in vitro diagnostic device work, with or without an AI focus, design and validation of electronic Case Report Forms, and registration in trial registries such as ClinicalTrials.gov. The scope includes advice on insurance coverage, SUSAR submissions, and medical writing. The contract period runs from August 1, 2026 to July 31, 2030, and orders placed during that window can continue afterward per individual agreements.