Reliable Clinical Data Management, From Start to Submission

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The Foundation of Reliable Research

At Kinesis, our Clinical Data Management (CDM) services are the bedrock of accurate and compliant clinical trials. We ensure that your data is not just collected, but meticulously managed, validated, and prepared to meet the highest industry and regulatory standards, providing a clear and trustworthy foundation for your research.

Why Kinesis for Clinical Data Management?

Choosing Kinesis for your CDM needs means partnering with a team dedicated to precision, compliance, and efficiency, providing you with data you can unequivocally trust.

Unwavering Precision
Our commitment to meticulous data validation and quality control ensures that every piece of data is accurate, complete, and reliable, minimizing errors and enhancing statistical power.
Regulatory Compliance Expertise
We operate with an in-depth understanding of global regulatory requirements (FDA, EMA, ICH-GCP), building databases and managing data in strict adherence to industry best practices for seamless submissions.
Proactive Quality Assurance
Beyond reactive checks, we integrate proactive quality assurance measures throughout the data management lifecycle, identifying and mitigating potential issues before they impact timelines or data integrity.
Advanced Technology & Methodologies
Leveraging cutting-edge EDC systems and innovative methodologies, we streamline data collection and management processes, enhancing efficiency and reducing operational costs.

Benefits for Your Clinical Team

Partnering with Kinesis for Clinical Data Management brings tangible advantages that optimize your resources and accelerate your research objectives.

Accelerated Timelines
Our efficient data management processes and proactive issue resolution shorten database lock times, enabling faster access to clean data for analysis and reporting.
Enhanced Data Quality & Reliability
By minimizing data discrepancies and ensuring consistency, we provide you with high-quality, reliable data that strengthens the integrity of your study results and regulatory submissions.
Reduced Operational Burden
We take on the complexities of data management, freeing your internal teams to focus on core research activities, thereby optimizing resource allocation and reducing overhead.
Regulatory Submission Confidence
Our adherence to global standards and rigorous quality control ensures your data is submission-ready, providing peace of mind and supporting successful regulatory approvals.

CDASH Compliant CRF design

Rapid study startup and database go-live

EDC configuration and validation

EDC configuration and validation (Medidata Rave, Veeva, etc.)

Medical coding (MedDRA, WHODrug)

Real-time data cleaning and query management

SAE reconciliation and external data integration

Vendor oversight and third-party data management

Database freeze and lock support

Compliance with ICH-GCP and 21 CFR Part 11

Your Data Deserves Precision.

At Kinesis, we don’t just manage data—we drive insights. Explore how our tailored biometrics solutions can elevate your clinical research.

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