ACRP Certified
Services
We Help You Deliver the Best Data
We serve as a support for clinical research sites, who conduct clinical trials.
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We develop Clinical Protocol, and train research sites staff for regulatory audit and inspections.
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See below for our full service offerings!
Clinical Research Site Start-Up:
A service for research naive doctors who'll like to conduct clinical research in their practices and don't have the knowledge of how to do it or where to even start. Full set up of the physical space and the operations development. One initial set up fee.
Data Quality Assurance Support:
A look inside your SOPs and study books to detect & correct any irregularities to be always audit ready and have peace of mind. Per hour charge or monthly fees available.
Data Collection Forms Development:
The development of Data Collection Forms that are study specific using study related documents and manuals to minimize the chances of visits mistakes and/or protocol deviations. Including but not limited to Study Visits, Study Logs, Study General Forms with notes to prevent study important study data points to be missed. Data Collection Forms amendments due to protocol amendments are included in the one time fee study set up.
SOPs that are created for your practice and research site. Personalized documents that apply to the way you do your research-related assessments. To guarantee that the data produce meets Protocol Requirements and Regulatory Guidelines. Study specific changes to SOPs are included in the one time fee initial site set up.
Procedures Development:
Standard Operating
Site Staff Training Support:
Initial site's staff training, training material and continuing education for Research Principal Investigators, Sub-Investigators, Research Coordinators, Regulatory Coordinators & Administrative Staff. Per hour charge or monthly fees available.