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 clinical 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 clinical 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