• ​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