
CLINICAL OPERATIONS
We design studies that are scientifically sound, operationally feasible, and regulatory-ready.
​​From strategy to site delivery
end-to-end operational oversight for every phase
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What’s Included
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Clinical trial startup and site activation management
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Monitoring (on-site, remote, and centralized) using RBQM methodology
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Investigator site support and training
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SAE management and safety reporting coordination
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Country, site, and patient enrollment forecasting
How CiNTL Pharma Adds Value
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Integrated oversight through cintl.ai for real-time operational tracking
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Adaptive monitoring using predictive analytics for early risk detection
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Seamless global operations supported by expert regional teams
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Outcome Faster startup, optimized site performance, and reduced operational risk across all trial phases.
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