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Clinical
Services Clinical trial design, Investigational Plan/Clinical Protocol Development
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Case
Support and Patient Selection
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Investigator
Brochures
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Case
Report Forms (CRF) & CRF Instructions
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Informed
Consent
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Site
Contracts, Investigator Agreements and Budgets
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Data
Management
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All Additional
Study Site & Investigator Documents
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Facilitation
of clinical sites including:
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Completion and submission of IRB / EC Documents IRB, Ethics Committee and In-Country Approvals Site selection, qualification,
initiation and close down visits Timely execution and successful management of clinical trials Site monitoring Data analysis and reporting CEC and DSMB Services
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Contracted Services
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Capitalizing
on regional expertise and minimizing travel costs, NCRG employs several contracted personnel around the world to monitor studies,
provide case support, provide data management, and to conduct statistical analyses. Our contracted suppliers are highly experienced
in First in Man, CE Mark and US IDE studies specializing in cardiovascular, neurovascular, pulmonary and orthopedic devices.
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