Feasibility & Patient Recruitment
D2V Clinical offers comprehensive site and enrollment feasibility services designed to facilitate successful clinical trials. Our expertise in feasibility assessments allows us to evaluate and identify optimal sites for your study, ensuring efficient patient enrollment and maximizing the chances of trial success. With a meticulous approach, we assess various factors including site capabilities, patient populations, regulatory considerations, and patient workflow. By leveraging our extensive network and industry experience, we provide sponsors with valuable insights and data-driven recommendations, enabling them to make informed decisions and optimize their trial design.
Our feasibility services include, but are not limited to:
Agency engagement
Our feasibility services include engaging with regulatory agencies to navigate the approval process, ensuring compliance and efficient communication throughout the study.
Site workflow
We meticulously evaluate site workflows, analyzing key logistical aspects such as patient recruitment, data collection, and study procedures to optimize efficiency, reduce potential bottlenecks, and enhance overall site performance.
Patient prevalence
Understanding patient prevalence is essential for accurate trial planning. Our feasibility services encompass thorough assessments of patient populations, allowing us to identify suitable sites with high recruitment potential and ensure a sufficient pool of eligible participants for your study.
Genomics
Harnessing the power of cutting-edge genomics technology, we integrate genomic data analysis into our research programs, providing valuable insights into disease mechanisms, biomarker identification, and personalized treatment approaches, driving advancements in precision medicine.
D2V Clinical gives you access
300+
GCP sites/hospitals
400M+
Patients accessed via hospital prevalence data
1M+
Principal investigators identified through hospital prevalence data