Our Services

Local and International Study Monitoring

Our Global Monitoring service ensures seamless oversight of non-clinical, Phase 1 clinical and development activities across multiple geographic regions. With an emphasis on quality, consistency, and compliance, we coordinate and supervise studies conducted locally and internationally to maintain alignment with regulatory standards, protocol integrity, and sponsor expectations.

VJO Canada provides:


  • Real-time oversight of all operational and regulatory activities across global sites


  • Harmonized reporting structures to streamline data flow and issue resolution


  • Consistent adherence to international regulatory guidelines (e.g., ICH-GCP, FDA, EMA, Health Canada)


  • Proactive risk management, with early detection and resolution of protocol deviations or operational challenges


  • Liaison support between sponsors, CROs, and investigative sites to ensure smooth communication


  • Audit readiness with comprehensive documentation and quality assurance practices


  • Cultural and logistical expertise, facilitating effective site engagement and coordination in diverse regions



By leveraging our global monitoring capabilities, you gain full visibility into your trial's progress, minimize delays, and ensure all study components align with your development goals—no matter where in the world they happen.