Clinical Trial Management

With years of experience in clinical trial design, Clintract offers a full range of clinical trial services including:

• Clinical Trial/ Project Management
        o Phase I
        o Phase II
        o Phase III
        o Phase IV/ Post Marketing
• Clinical Monitoring
• Medical Writing
• Protocol Development
• Informed Consent Form Development

• Adverse Event/ Serious Adverse Event Reporting

• FDA Submissions:
        o IND
        o NDA
        o FDA 1571
• IRB Submissions
• Principal Investigator/ Clinical Site Recruitment
• Patient Recruitment
• 3rd Party Contract management and investigator reimbursement

Our global footprint allows us to recruit sites, patients, and investigators in countries around the world and tailor specific monitoring services for your study.

With some of the world’s leading scientists as well as skilled and experienced technicians on staff, Clintract has the deep therapeutic expertise you need for successful trials in oncology, cardiology, neuroscience, dermatology, ophthalmology, and other therapeutic areas.

The right size and custom fit for your trial needs – that’s why when it comes to phase clinical trials, Clintract works for you.

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