Services
Our Services
We Execute Clinical Trials
We offer a comprehensive range of services designed to support every stage of your clinical trial journey. From protocol feasibility and regulatory documentation to patient recruitment and site management, our experienced team is dedicated to delivering high-quality, patient-centered research solutions.
LOCATE NEW STUDIES
We will assist you in the identification and place of new studies at your facility.
ACCOUNT MANAGEMENT
We will tract accounts receivable for work performed on studies at your facilities, and provide billing sheets for each visit during the study duration.
PROTOCOL FEASIBILITY
We complete your feasibility submissions to Sponsors for new studies based on your patient population and facility.
REGULATORY FILE MAINTENANCE
File, organize and maintain all regulatory files digitally to comply with FDA, Sponsor, and IRB guidelines.
CONTRACT/BUDGET NEGOTIATION
We will negotiate with the Sponsor Company for the Clinical Trial Agreement regarding the new studies placed at your site
REGULATORY DOCUMENTATION
We complete the initial regulatory documents for new studies based on your site