Business Models
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Site Management & Monitoring
Biostatistics
Institutional Review Board (IRB)
Full-Service Model
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CEERI has the resources and capabilities to undertake most clinical trial projects internationally and act as a full-service Contract Research Organization (CRO)
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The full-service model is ideal when pharmaceutical companies/sponsors have limited resources and deployment of additional staff is costly or impractical
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In this model, CEERI contracts with medical institutions to conduct clinical trials
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Clinical Trial Agreement (CTA) and payments are between CEERI and the medical institution. CEERI commits to payments and is paid by sponsors
Functional Service Provider Model
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The Functional Service Provider (FSP) Model is ideal when pharmaceutical companies/sponsors only need assistance in certain functions or geographic locations or need additional staff to support current in-house departments or functions
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FSP is very flexible and varies from project to project
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All contracts, payments and legal framework are executed by two sets of agreements:
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Master Service Agreements (MSA) that deals with the general deliverables
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Statements of Work that deal with specific parts and sections
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Hybrid Model
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The Hybrid Model deals with the structural and support gaps between pharmaceutical companies/sponsors and Contract Research Organizations (CROs) on one side and investigators and sites on the other
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We embrace the Hybrid Model that emphasizes Contract Reserach Organization (CRO)/Site Management Organization (SMO) support systems in several international locations in central and eastern Europe
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The Hybrid model enables CEERI or any of its affiliates to completely compliment sponsors’ resources to manage studies, whether they have another CRO or they manage the study without a CRO