Porta Clinica offers collaborative consultation across a range of clinical investigation and translational drug development projects, including participation in the design, conduct, and analysis of clinical trials of all phases.
Independent Medical Monitor services, participation in independent Data Safety Monitoring
Board (DSMB). protocol design, and provision of medical consulting in close collaboration with regulatory personnel in your organization in the drafting
of regulatory submissions, expedited safety reports for ADRs, SAE report narratives,
analysis of study results, and review and analysis of complete study reports are the most frequently engaged consultation activities.
Porta Clinica has collaborated successfully in an independent consulting relationship with a number of different academic, biopharmaceutical, pharmacovigilance, non-profit research foundations, and contract research organization groups.
