Veritas IRB

Ethical feasibility

Our team of research professionals and consultants, as well as members of the Veritas IRB board, can assist you with the development of innovative study designs and procedures by providing you with an initial ethics feasibility assessment.

Feasibility assessments allow you to benefit from the insight of the IRB at the developmental stage of your study protocol. You obtain valuable information that ensures that your protocol is developed in accordance with applicable research ethics requirements such as minimizing risks of harm and maximizing benefits, respecting research participants' autonomy, and protecting their privacy and confidentiality.

Veritas IRB has conducted numerous feasibility assessments including those involving the following areas of research:

  • Conduct of clinical trials in emerging countries
  • Retrospective use of stored tissue samples
  • Recruitment of employees for research purposes
  • Innovative placebo-controlled trials
  • Clinical trials involving alternative medicine procedures

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