SCR can perform phase I-IV clinical trials in the following therapeutic areas and we continue to increase our capabilities.
- Screen to fail rati o is 15-20%.
- Average enrollment/study approximately 20 subjects.
- IRB timeline for approval is 1wk.
- Budgets, Contract negotiation completed within a week.
- Access to local IRB and can work with institution IRB if required.
- EHR access.
- ICH-GCP Certification.
- Can carry out most phase I-IV.
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