Pharmaceutical companies may establish endpoint or adjudication committee to review the study safety or efficacy endpoint, particularly when the end points are subjective and or complex.

Our team has decades of experience in managing clinical data from Phase I to IV in different Electronic data capture systems and legacy paper CRF models across several therapeutic areas.

We help pharmaceutical and biotech companies to better manage clinical trial by providing modern cloud based electronic Trial master file (ETMF) solutions.

With more than Decade of experience delivering consistently high quality, medical writing experts ensure that your Protocol, Medical Narratives, dossiers, and other key materials are clear, concise, scientifically accurate and fully compliant with regulations, and industry best practices.

Exciting innovations in data analysis and visualizations are paving the way for a better clinical experience.