Data Management & EDC

Data Management & EDC

Tranquil Clinical Research offers complete Data Management services to best fit each client’s needs and budget. Data Management is a key component of the clinical study to ensure reliable and efficient data collection as well as availability of data for analysis.  At Tranquil Clinical Research we allow innovation and creativity to drive how we proffer solutions for our clients. We ensure your EDC system meets the FDA GCP 21 CFR Part 11 compliance requirement for all our clinical trials. Our EDC systems have capabilities for:

  • User Acceptance Testing
  • Serious Adverse Event reconciliation
  • Medical coding
  • Data export
  • Functional reporting tools

Our experts will analyze your study design and budget to make the best recommendations for an EDC platform to best serve your needs. Reach out today to find out how Tranquil Clinical Research can implement our strategies for efficacious management of your data!

Tranquil Clinical Research is in the business of innovation, servicing sponsors, patients and clients through clinical trials.


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