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Principal IRB reviews the following types of research studies: 

  • Review of Phase I-IV Biomedical Research, Single and Multiple Investigator

  • Review of Government Sponsored Research as Identified in CFR, Title 21, Parts 50, 54, 56, 312, 812 and Federally Funded Research as Identified in CFR, Title 45, Part 46

  • Review of Medical Device Research

  • Review of Social and Behavioral Research

  • Review of Stem Cell Research

  • Review of Consumer Preference, Observational and Registry Research

  • Review of Investigator-Sponsored Research

  • Review of Research in Academic Settings

  • Review of Research in Hospital Settings

  • Review of Projects That May Be Exempt From Federal Regulations

  • Review of Compassionate Use Research

  • Expedited Review of Studies as Identified in the Federal Register

  • Expedited Review of Investigators Involved in Multiple-Investigator Study

Principal IRB also Provides the Following Services:

  • Pre Review of Submission Documents

  • As-Needed Emergency Meetings

  • Revisions and Maintenance of Approved Informed Consent Documents

  • Multi Site Reviews with a Single Point of Contact Throughout Your Study

  • Document Translation

  • Consultation, as Requested

  • Competitive Pricing

  • Quality Assurance/ Quality Control

  • Flexiblity to Meet Your Specific Needs

  • Eco Friendly and Paperless Review

  • 21 CFR Part 11 Compliant Electronic Document Management System (Launch)

  • IRB Documents within 1 - 2 Days of IRB Review

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