Biomapas works directly with clients to design feasibility studies that are tailored to the needs of a planned clinical trial or clinical research program.
Each study includes both medical and regulatory reviews to identify study-related opportunities and risks in each country. For every project, a Feasibility Coordinator is appointed and supported by dedicated local CRAs, who manage feasibility studies in individual countries. The performance of such an assessment allows us to find the optimal and most cost-effective solution for our clients.
Highly motivated investigators as well as timely and sufficient patient recruitment are crucial in order to succeed in every clinical trial. Biomapas has an extensive network of investigators, with long-standing relationships. This allows quick access to Key Opinion Leaders or Principal Investigators across a broad range of therapeutic indications and enables us to better predict the success rate of the clinical trial.
Feasibility Study Service
Strategic feasibility assessments that guide the site selection process and the recruitment planning include:
- First contact with potential investigators and a survey-based evaluation of their interest;
- Site qualification visits;
- Evaluation of potential patient pool in each country and in-depth analysis of patient recruitment associated risks;
- Analysis of competitive trials;
- Analysis of country-specific regulatory requirements, treatment practices, importation/exportation procedures, etc.;
- Assessment of patient and physician willingness to participate in the study;
- Assessment of site capabilities and experience.