Our main purpose is to help the Pharmaceutical Companies and Contract Research Organizations to find the right Physician Investigator to assure the rapid and accurate completion of the clinical trial.
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Our quality focused approach commands continuous innovation and flexibility both at investigative sites and in-house. The VID Research Concept team create and customised site management programme for the successful delivery of the smallest of studies through to large complexed studies involving multiple sites with specific needs.
VID Research Concept has strong and established relationships with its investigative sites across the country and close interaction with health and delivery processes enables new insights and solutions, practical support, site specific planning and the realisation of site specific goals. The vid concept team provide an exclusionary questionnaire to all our partners and that is the first step in our professional relation.
Our study co-ordinators and research nurses have a clear focus on enabling a consolidated study duration and exceptional site performance including speed, reliability, productivity and data quality. By deploying such resource this affords greater efficiency, benefits and a balanced partnership between the clinical trial process and patient management.
The process of running a clinical trial from the very point at which the data are live when the patient and the study interface, right the way through to the production of a final report is managed with the highest quality standards and professional integrity.
Preliminary Screening
Our initial screening begins with a comprehensive site/staff background check that includes CV reviews, medical license
verification, and state medical board and FDA audit checks with thorough review of all 483s. Clinical research abilities
are rated based on several criteria, such as:
Study Pre-qualification
For each study, we identify appropriate sites based on protocol requirements and sponsor preferences. Upon collection and
review of study-related documents (CDAs, Questionnaires, CVs, etc.), we submit completed documents for the most qualified
investigators. Sponsors make the final site selection decision, communicating directly with site personnel for further
qualification and contract negotiations.
Ongoing Monitoring
ISS site performance is monitored on an ongoing basis by continually analyzing site-reported data and statistics from our
internal tracking systems. Periodically, our staff will check in with the sponsor/CRO for site selection confirmation,
enrollment data, and performance feedback. By assessing issues such as patient recruitment and retention, site compliance,
and document turnaround times, we can continue to ensure overall site quality.