Data Management
What This Service Include
Our Data Management systems implement various statistical analysis methods for testing and comparing pharmacokinetics parameters. Based on our accumulated experience, we have been able to develop several statistical analysis methods for testing, comparing, and validating Pharmacokinetic parameters. Our QA / QC teams ensure that all data and reports are managed according to detailed SOPs and international guidelines.
What Sets Us Apart
Years in
the market
More than 22 years in the market.
Healthy
volunteers
More than 3000+ healthy volunteers.
Bio Studies Conducted
Over 800+ Bio Studies Conducted.
Validated
assays
Over 300+ validated
assays.
Our Services Include
Protocol Writing and Design.
CRF Design
ICF Translation
Statistical analysis via Kinetica TM
and SAS
Final Reports
Sample Size Estimation and Randomization
Our Quality Guarantee
It is of paramount importance when establishing clinical trial centers that a rigid quality system is in place with standard operating procedures (SOPs) carefully created and tailored to fulfill the procedural requirements. At JCPR rigorous regulations exist surrounding every aspect of the center from the design and setup to documentation, storage, health and safety, and reporting. Specialized training is also required from the analysis and operation of the equipment to documentation and generation of reports.
In partnering with our clients and investing in the well-being of our staff, employees, and Volunteers. We at JCPR have spent the good part of our last 30 years establishing and developing a quality system that enables us to run studies as per national and international guidelines smoothly. JCPR is always under constant development. Especially that our center is one of the very few centers in the region that is completely and totally independent without any external benefactors or shareholders. This is one of our many advantages to ensure transparency, integrity, and ethicality in this industry.
