
Solutions
Early Development, Clinical Trials, Surveillance & PMO Consulting Services.
At Cintl Pharma we harness the power of data to optimize every facet of drug development lifecycle. We help guide your projects throughout the drug development journey. Not just standard, bespoke FSP 360 models to expedite any project or program irrespective of size.
Our Services
Explore CiNTL Pharma expertise, where our professionals harness the power of data to optimize every facet of your projects throughout the drug development journey.
Risk-Based Clinical Monitoring
Our risk-based clinical monitoring services help ensure the safety and efficacy of your clinical trials. By utilizing data-driven solutions, we are able to identify potential risks and implement proactive strategies to mitigate them.
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Clinical Operations
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Data Management
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Quality Assurance Management
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Project Management
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Vendor Management

Early Research Development
•Plan/Execute/Deliver Protocol Strategy
•Patient Recruitment & Enroll Strategy
•Supply & Procurement Strategy
•Regulatory Submission, Approval & Compliance Strategy
•360 Data Driven Strategy
•KOL Strategy
•Scope/Drug Manufacturing Strategy


Project and Data Management
At CiNTL Pharma, we understand the importance of efficient project and data management. Our team of experts will work with you to ensure that your clinical trials are conducted smoothly and that all data is collected and managed in a secure and compliant manner.
Statistical Analysis
Our statistical analysis services help you make sense of the data collected during your clinical trials. We use advanced statistical methods to provide you with accurate and meaningful insights that can inform future decision-making.
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FDA Review, FDA Approval and Post Approval
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Regulatory Compliance
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Drug Safety
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Outcomes Research/Analysis
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Market Access Strategy & Execution
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Supply Chain & Procurement
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Drug Manufacturing& Packaging
