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We provide direction and operational leadership for all stages of clinical research studies to ensure delivery on time, within budget, and of high-quality in compliance with ICH GCP, Internal Standard Operating Procedures, and all other applicable regulations.

Certa Victoria Scientific offers full service clinical research management but can also work with you in your area of need as listed below:


  • Clinical Research Development    
  • Collaboration Development
  • Community Engagement in Research
  • Funding and Sponsorship Guidance
  • Regulatory Guidance
  • IRB Application
  • Study Protocol Development
  • Informed Consent
  • Waivers
  • Site Monitoring
  • Principal Investigator Recruitment
  • Patient Enrolment
  • Orphan Drug Application       
  • Rare and Orphan Disease trials