Once the design of the clinical investigation is defined, MSOURCE will ensure translation into the appropriate clinical investigation protocol and data capture possibilities with valuable input by medical writing team.

MSOURCE offers:

  • Input into the design of your clinical investigation
  • (e)CRF design, database set-up and validation
  • Electronic data capture
  • Flexibility to work on your data management systems
  • 21CFR11 compliant solutions
  • Data integration from laboratories or specialist data collection devices (ECG) or analysts (Central Imaging)
  • Support to DSMB and CECs
  • Data quality appropriate to your objectives