ethica CRO


Data Collection

Electronic data collection is used on an increasingly routine basis for clinical studies. However, depending on the nature and scope of the study, as well as the budget, other data collection formats may be more appropriate. We are equipped and experienced in collecting study data using a variety of formats including:

  • electronic (eCRF)
  • paper
  • interactive voice response (IVR) systems
  • facsimile

Based on the Sponsor's needs, we provide regular biometrics reports of routine study parameters such as:

  • screening/enrollment status
  • CRF status
  • study medication inventory
  • investigator payments
  • adverse events (AEs)
  • primary/secondary outcomes

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ethica Investigator Manual