Feasibility Assessment
Using our experience to help you expedite your study initiation.
What we do
At Orizzonte, we recognise that a thorough feasibility assessment is pivotal for the successful initiation and execution of a clinical trial. A well-conducted feasibility assessment helps identify potential challenges and opportunities, ensuring your study is set up for success from the start.
Why Choose Orizzonte for Feasibility Assessment?
Our team of experienced clinical operation professionals and research specialists are dedicated to providing a comprehensive feasibility assessment tailored to your study’s specific needs. Our services include:
Site Evaluation: Conducting detailed assessments of potential sites to determine their suitability based on factors such as infrastructure, patient demographics, and investigator experience.
Resource Assessment: Evaluating the availability and capability of necessary resources, including personnel, equipment, and facilities, to support your trial efficiently.
Regulatory and Compliance Review: Ensuring that all regulatory and compliance requirements are met by reviewing local regulations and guidelines pertinent to your study.
Risk Identification: Identifying potential risks and obstacles that could impact your trial’s success and providing strategic recommendations to mitigate these risks.
Feasibility Report: Delivering a comprehensive report outlining our findings, including site capabilities, potential challenges, and recommendations for optimal study design and execution.
Partnering with Orizzonte means benefiting from our expertise in evaluating trial feasibility, ensuring that your study is strategically positioned for success. With our support, you can move forward with confidence, knowing that potential challenges have been addressed and opportunities maximised.