Data Management and Statistics

agile Clinical Research offers a full spectrum of data management services and expertise to analytics-cropensure the efficient and appropriate management of your clinical trial data. Our team is experienced in clinical trial design, implementation and execution at all levels. They are well trained and rigorously follow Standard Operating Procedures (SOPs) that encompass HIPAA security, industry regulations, HIPAA compliance, engineering and GCP. Using state-of-the-art data management, data analytics, business intelligence system technologys, we are able to deliver a high-quality, master data database.


Our services include:
  • Data analytis, CRF and database design
  • Medical coding and reporting
  • Clinical trial HIPAA safety database/ reconciliation
  • Lab data import and reporting
  • Maintain MDM (Master Data )
  • Remote Electronic Data Capture and maintain hight availability database
  • Provide 24x7 data availability for analytics and BI reporting
  • Data validation, storage and archiving
  • Biostatistics using statical models

All statistical analysis is done with SAS® software. For special statistical tests, customized software applications used. This set of special tests is completely integrated into SAS and Qlikview.

Our primary aims are accuracy, clarity, consistency and quality. We recognise the importance of effective communication in the achievement of your research objectives.