FARMOVS Project Management Division
Building lasting relationships accross the globe
Our experienced team of project managers oversee Phase I–III clinical studies for local and international clients. We build lasting relationship with our clients and service providers by valuing each role-player, firmly believing that the contribution of the entire team leads to the success of a study. The project managers ensure open and timeous communication regarding the milestones and status of each project and deliverable and strive to achieve the highest level of client satisfaction.
The FARMOVS project management team offers the following:
• Management of Phase I studies, from initiation to close-out, including FIH and Healthy Volunteer Bioequivalence and Bioavailability studies, in close collaboration with the principal investigator and clinical team
• Full-service project management, requiring the oversight of the study across all phases; i.e., from protocol preparation and submission to Regulatory Authorities, clinical conduct, bioanalysis, data management and biostatistics to report writing, in close collaboration with all role-players and service providers
• Filing of essential documents and maintenance of the investigator site file, as well as support with the compilation and maintenance of trial master files (including on-site archiving after study close-out)
• After study support, i.e., assistance with regulatory queries following dossier submissions