Clinical Data Management, Analysis and Reporting

Clinical trial databases go into production on time 94% of the time

Seamless integration of clinical data through synchronized platforms

Stand-alone, full-service or functional outsourcing models

The Fortrea team masters multiple disciplines and technologies for one purpose — to lock your database as soon as possible

Clinical data management.

You may engage us for stand-alone, full-service or functional outsourcing in the following disciplines:

  • Protocol design & review
  • Randomization schedules
  • Case report form (CRF) design & review
  • Database design
  • Data entry
  • Data validation / verification
  • Data transfer
  • Medical coding
  • Quality management procedures
  • Data manipulation
  • EDC


Consistent clinical data regardless of geography.

There are myriad moving parts within complex, global clinical trials. Using common global platforms and harmonized processes, we are able to assure you that you have the highest data quality, worldwide. Fortrea provides accurate clinical data from the moment it is recorded to the time that it is reported.

Your data never goes to sleep...nor do we.

Our global infrastructure, workflow and informatics platform give you the benefit of a 24-hour clock. And, since our teams are all trained and comfortable with the same processes, you’ll benefit from global team interchangeability.

End-to-end clinical data management, analysis and integration.

Having the internal sources to manage all the data a clinical trial generates can be difficult. Fortrea assists you with clinical data management every step of the way — from the point it is first collected to warehousing it. Fortrea has a specialized and dedicated team responsible for coordinating both internal and external communication. This enables easy access to subject matter experts and higher quality output, every time.

Statistical consulting.

We help you define correct study components for optimal efficiency, then follow through to ensure clinical results meet your goals.


Advanced programming solutions improves efficiencies, in one study or across many studies:

  • Statistical analysis plans
  • Integrated summaries for safety and efficacy
  • Tables, figures and listings
  • Randomization code generations
  • Statistical and clinical study reports
  • Publication and abstract support


Clinical data analysis services.

  • Pharmacoeconomic and QoL analyses
  • Mid-study evaluations including interim analysis


Integration and warehouse design.

  • Data safety monitoring boards (DSMBs)
  • Setup, charter, analysis plan development and maintenance

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