Services | Portfolio

• Monitor time, cost &, quality
• Coordinate team, customer & vendors communications
• Perform risk management
• Provide training

• Feasibility and study set up
• Site selection
• Support for patient recruitment and retention
• Site management

• Submissions to IRBs/IECs
• Submissions to local Regulatory Authorities
• Import/export of study materials

• ICH/GCP
• Local regulations
• Protocol specific

Successful clinical trials depend heavily upon providing study supplies to the correct study site physician at the correct time. KLIXAR can provide the project management resources and technical expertise that our customers need to be successful. By hiring KLIXAR's Clinical Study Supplies Logistics you would be getting the following strengths:

• Experienced Clinical Trial Management Teams that will remain on your project throughout the duration of your study.

• A dedicated project leader who streamlines communications on the the parties involved.

• We also offer insight into the ever-changing regulatory environment; and the ability to support your needs from strategy through execution.

• A net of depots throughout Latin America.