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A feasibility study is an evaluation of a proposed study protocol to determine the difficulty in carrying it out. Generally, a feasibility study precedes technical development and project implementation. In other words, a feasibility study is an evaluation or analysis of the potential impact of a proposed protocol.
Accovion conducts clinical trial feasibility studies to provide you with information regarding:
- Research environment and infrastructure
- Regulatory, medical and regional requirements
- Local regulatory and ethics review timelines
- Compatibility of the protocol and assessments with current standard of care
- Potential modifications to clinical trial design and eligibility criteria to enhance enrollment and execution
- Competing clinical trials
- Availability of the targeted patient population
- Investigator interest in the clinical trial concept.
- Site capabilities
- Personnel
- Equipment
- Grant management requirements
- Contractual requirements
- Projected patient enrollment rates
Accovion works directly with you to design a feasibility study that is appropriately tailored to your planned clinical trial.
Feasibility report
Besides providing data to support decision making, the Accovion feasibility report includes clear, data-driven operational strategy recommendations for the successful conduct of your trial. The report indicates potential risks and our Medical Services experts can help you with effective strategies to mitigate them, right before start-up activities begin.
Dr. Andree Beckerling
Senior Medical Director
+49 6196 7709-343