Clinical Research Consulting
Cureline Clinical Consulting Partners (CCCP) is a clinical research consulting group offering cost-effective and time-sensitive solutions for conducting clinical trials at the premier linical sites and research institutions in Russia and the former Soviet republics. Through our network, CCCP also offers clinical trials auditing, regulatory affairs, site monitoring and project management services in the USA, South Africa, Israel, India, and the Philippines.
CCCP was formed by Cureline Inc., to leverage already established effective collaborations for biosample procurement services with linical sites and research institutions. Through our clinical site network we offer to our clients:
- Expedited start-to-completion study time
- Patient recruitment capabilities including access to naïve patients
- Competitive pricing
Clinical Research Services
Clinical Trial Management
- Site selection, qualification and initiation
- Regular site visits and monitoring
- Source data verification and query resolution
Clinical Trial Auditing
If your organization has an open clinical protocol that has serious troubles with patietns' enrollment, we can evaluate the protocol, inspect clinical sites conduct, interview with current and potential Principal Investigators and provide recommendations for the study improvement.
Regulatory Affairs
- Preparation of all required regulatory documents and submission packages
- Local ECs/IRBs approvals
- Import/Export approvals
- Local patient insurance policies
- Drug labeling
Clinical Contract Staffing
CCCP has well-established relationships in the clinical research community and has the capability to recruit and assign to projects well-qualified employees (CRAs, Project Managers, Data Managers, etc.)
For detailed information about CCCP clinical research service, visit our website at www.CCCPtrials.com
