2uCDM Data Solutions
To be a leading force in clinical data management, driving innovation and excellence in clinical research to improve global health outcomes.
To provide exceptional consulting service in clinical data management that ensure data integrity, compliance, and efficiency. We aim to support our clients in achieving their research goals through innovative solutions, expert guidance, and a commitment to quality.
Welcome to 2uCDM Data Solutions, consultancy firm founded by Ullas Arabhavi.
With nearly 20 years of experience in Clinical Data Management (CDM), the pharmaceutical industry, and academic research, we excel in maintaining the highest standards of data integrity and compliance. Our commitment is to ensure the highest quality in clinical trial data and adherence to industry standards and regulations. At 2uCDM Data Solutions, we are dedicated to providing meticulous attention to detail and innovative solutions to meet the data management needs of Pharma/Biotech companies, Contract Research Organizations (CROs), and Functional Service Providers (FSPs).
By offering tailored CDM solutions, we strive to deliver robust and reliable results for every project. Join us on our journey to elevate the quality and integrity of CDM service provision, supporting your unique requirements.
Ready to elevate your data management? Let’s make it happen with us
We enhance efficiency and cost-effectiveness in CDM through tailored business optimisation strategies, streamlining processes to ensure top-tier performance and regulatory compliance.
We specialize in developing and executing comprehensive CDM strategies, focusing on continuous process improvement to elevate data quality, reduce risks, and maximize project success for clients.
We navigate complex regulatory landscapes, ensuring compliance and smooth submissions to regulatory authorities through expert guidance and support.
We provide comprehensive CDM documentation services, creating precise and compliant documentation essential for clinical trials and regulatory submissions.
We help implementation of robust Quality Management and Risk-Based Quality Management (RBQM) frameworks, enhancing data integrity and minimizing risks throughout clinical trials.
We streamline data integration processes, ensuring seamless and accurate aggregation of clinical data from multiple sources for effective analysis and reporting.
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To be a leading force in clinical data management, driving innovation and excellence in clinical research to improve global health outcomes.