Veritas IRB has the expertise to review and oversee all phases of clinical research involving drugs, biologics, medical devices and natural health products, as well as genomic research and research involving behavioral and social sciences.

Veritas IRB provides the following services as part of its standard ethical review and oversight program:

• Clear approval forms identifying documentation reviewed and decisions taken on each document reviewed
• Preparation and production of informed consent documents following IRB review at no additional costs
• On-call consultation from our knowledgeable staff on all aspects of study submission and review at no additional costs
• 24-hour, toll-free, bilingual research participants’ hotline where our knowledgeable personnel answer questions    regarding research participant’s rights and Investigator’s obligations
• Free access to user-friendly guidance documentation on ethical conduct and Good Clinical Practices. 
  

The following services are also available:

• Priority review meetings
• Ethical feasibility assessments
• Certified translations of approved documentation
• Consultation on research ethics and Good Clinical Practices 
• Education and training on research ethics and Good Clinical Practices
• Human Research Protection Program development
• Auditing and monitoring of IRBs
• Submission management to University- or Hospital-affiliated IRBs.