Optimizing Clinical Trial Success from the Start. At Ardent Clinical Research Services (ACRS), we recognize that successful site selection begins with robust feasibility planning. Our Feasibility and Site Selection team plays a pivotal role in ensuring that every clinical trial is placed at the right site with the right investigators, helping to drive recruitment efficiency, regulatory compliance, and high-quality data collection.
Feasibility isn't just a step — it is a strategic function integrated into our project planning and proposal development process. Before a study begins, our team evaluates trial-specific parameters to ensure alignment between protocol requirements and site capabilities.
We conduct thorough evaluations based on:
Our goal is to identify top-performing, protocol-ready sites that can initiate quickly and recruit effectively.
Our feasibility specialists have worked across virtually all therapeutic areas, including oncology, neurology, cardiology, gastroenterology, infectious diseases, and more. Their experience enables faster and more accurate site matching based on therapeutic fit.
We maintain direct relationships with a wide network of investigators and trial sites across India and globally. This enables rapid outreach, early engagement, and honest feasibility feedback.
Our dedicated Feasibility & Site Selection Managers personally visit the shortlisted sites to:
This hands-on evaluation ensures the real-world readiness of each site to execute the trial as per protocol.
Choosing the right sites from the beginning can save time, reduce costs, and minimize protocol deviations. At Ardent, our targeted and data-backed feasibility process ensures that your clinical trial is built on a strong foundation for success.