Data Management

Customized Solutions For Each Study

MedTrials’ goal is to provide customized data management solutions that are right for you. With a management team that has an average of 30 years of industry experience, we recognize that every client is unique and every study is different. We believe that data management solutions should be customized to satisfy client, regulatory, and scientific needs. Through innovative data management solutions, MedTrials partners with you to ensure that the information generated from your data is valid, reliable, complete, and accurately reported.

MedTrials integrates a skilled team of data management professionals into the project development process as early as possible. This approach builds team identity and communication and promotes early collaboration in order to provide high-quality data that is accurate, accessible, and ready for analysis in a cost-effective and timely manner.

Services include:
  • Electronic data capture (EDC) system selection and deployment
  • Serious adverse event reconciliation
  • Design and development of CRF/eCRF and CRF completion guidelines
  • Independent user acceptance testing
  • Vendor management and data reconciliation
  • Data verification and cleaning consisting of both manual and electronic review
  • Management, generation, resolution, and tracking of queries (DCFs)
  • Interim closures as specified by project
  • Dictionary coding using standardized dictionaries (MedDRA, WHO-drug)
  • Standard and customized metric reporting
  • Development of customized data reports
  • Standard or customized data transfers
  • Integration of external data (laboratory, ECG, other)

Data Management

Through comprehensive data management solutions, MedTrials partners with you to ensure that the information generated from your data is valid, reliable, complete, and accurately reported.

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Biostatistics

MedTrials careful biometric planning and execution promoted evidence-based solutions from valid, reliable and well-represented data.

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Safety

Safety reporting is a critical component of clinical trial management. A partnership with MedTrials offers a full range of safety support services.

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Medical Writing

MedTrials offers well structured and detailed writing services ranging from individual documents to extensive medical writing programs.

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Question About MedTrials Services?

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