Clinical Trial Unit

Mission:

To bridge the gap between research and real-world impact, ensuring equitable access to innovative treatments, particularly for underserved populations.

Objectives:
  • To generate high-impact research; produce evidence-based results and publish findings to contribute to general knowledge.
  • To promote ethical research practices; ensure all trials meet the highest ethical standards and maintain transparency and compliance.
  • To enhance healthcare access; focus on diseases prevalent

in the community, and develop affordable therapeutic solutions

  • To foster collaboration and innovation; build strong partnerships with national and international research institutes, pharmaceutical companies, and government bodies.
  • To empower communities; Increase awareness of clinical trials through education and outreach.

At KIRCT, we offer clinical trial logistics which include;

  1. Pre-Trial Logistics
  2. Study Materials Preparation
  3. Regulatory Documentation
  4. Site Setup

 

  1. Initiation Phase Logistics
  2. Shipping of Investigational Products and Supplies
  3. Centralized Laboratory Services
  4. Site and Investigator Readiness

 

  1. Conduct Phase Logistics
  2. Patient Enrollment and Coordination
  3. Investigational Product (IP) Dispensation
  4. Logistics of Monitoring and Visits

 

  1. Data Management and Analysis Logistics
  2. Data Collection Systems
  3. Interim Analysis Logistics (if applicable)

 

  1. Close-Out and Completion Phase Logistics
  2. Final Data Collection and Reporting
  3. Return of Supplies and IP
  4. Regulatory Reporting and Submissions

 

  1. 6. Post-Trial Logistics
  2. Long-Term Follow-Up and Monitoring (Post-Marketing)
  3. Archiving