QUALITY DATA FOR BETTER OUTCOMES

Comprehensive CDM Compliance Meeting Regulatory and Industry Standards such as CDISC& CDASH, 21 CRF Part 11, ICH E2A, GDP, and HIPAA

RIGHT DATA FOR EXPEDITED PRODUCT REGISTRATION

Our CDM experts work closely with clinical trial teams to collect complete, accurate, and free from inconsistencies, which helps to boost confidence of stringent regulatory agencies and secure marketing authorization.

  • eCRF design
  • SAP Development
  • Statistical Analysis
  • TLFs
  • ADaM / SDTM
  • Standards Consulting
  • Database development and testing
  • Data entry and tracking
  • Database closeout and archiving activities.
  • Discrepancy management
  • External data reconciliation
  • Medical coding
  • Lab safety data and Biomarker data management.

With our CDM services, you can be assured of high-quality data to support regulatory submissions for marketing applications for your new medical products. Partner with us to ensure the success of your clinical trial

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Make a difference in patients’ lives by setting your clinical trial on the path to success today.