Clinical Trials

Clinical Trials – Management and Services

Pacific-Link Consulting provides clients with a flexible, best-in-class approach to improve cycle times, constrain costs and reduce risks. Specializing in the planning, management, execution, and analysis of clinical trials, ranging from small studies to large, complex, multinational projects, and supported by an experienced study group, the team at Pacific-Link is able to apply our therapeutic, regulatory, and operational expertise to consistently solve the challenges that arise during clinical projects.

Our expertise extends to all aspects of Clinical Trial Management:
Early Phase

• Clinical PK/PD
• First in Human
• Early Product Development
• Data Monitoring Committee

Late Stage

• Patient Recruitment
• Study and Project Management
• Monitoring
• Data Management and Statistics
• Vendor Management
  • Clinical Supply
  • EDC/Patient Reported Outcomes
  • Lab
  • Imaging
  • IVRS/IWRS

Other Clinical Trial Services

Pacific Link Consulting can file Clinical Trial Applications (CTAs) in Canada on a clients’ behalf. We can help the client obtain legal authorized representative for the region, project manage your CTA, write and prepare meeting requests as well as meeting packages.

Pacific Link can also assist the client with clinical trial data management, clinical trial monitoring and clinical protocol development.

Other markets of expertise include Japan and Europe.

Please contact us to learn more about what Pacific-Link Consulting can do for your project.