Who we are | Why verum

The high level of education among our staff (80% academics and physicians) and our crosscultural expertise make Verum a reliable, professional partner. For decades, Verum’s organization has aligned with modern trends and clients’ requirements for clinical trial management and quality. Between 2000 and 2019, 32 drug candidates reached marketing authorization, and Verum staff successfully completed 47 audits and regulatory authority inspections (including FDA and EMA) without critical findings.

Our indepth knowledge of national regulatory requirements and local specificities enables us to prepare and submit CTAs efficiently, minimizing requests for additional clarification from authorities and securing approvals within an acceptable  timeframe.

Verum has implemented a quality management system based on ISO principles, with a strong focus on data reliability to ensure that trials are conducted and data are generated, documented, and reported in full compliance with the protocol, GCP, and regulatory requirements. The QMS is underpinned by comprehensive SOPs, up to date policies, experienced QA personnel, and ongoing  training  programs.

With our deep expertise in clinical trial budgeting and a clear understanding of project resource needs, we provide clients with cost effective, realistic project planning that minimizes the risk of hidden or additional  costs.