At Vita Global Sciences, we understand the importance of clinical data assets in the pharmaceutical, biotech and medical device industries. Our expert team is committed to ensuring that your clinical trial data management process: 1) fits your project needs, 2) is highly efficient, and 3) meets the highest standards of integrity and quality by complying with Good Clinical Data Management Practices (GCDMP) and Clinical Data Interchange Standards Consortium (CDSIC) requirements. A team of highly experienced data managers will support all CDM-aspects of our project, individual trial databases are developed according to your business requirements, data is being consequently monitored and validated prior to transfer to the formulation level.
Our core competencies in data management comes from our thorough knowledge of standards, our flexible systems, and the effective use of vividly available data management systems.
Our Clinical Data Management Services Include
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Data Management Trial Master File Set-up and Maintenance
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CRF Design and Development
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Clinical Database Design and Development
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Data Cleaning
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Data Quality Control Audits
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Edit Check Programming, Validation and Testing
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Medical Terminology Coding (MedDRA and WHO drug)
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Independent QC Review
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SAE Reconciliation
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Query Generation and Reconciliation
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Database Lock
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Applications (e.g., EDC, IRT, ePRO, eCOA)
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Decentralized Clinical Trials
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Clinical Data Configuration
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Apache Spark (databricks)
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Biomarker Data Management Support
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Study Build & Libraries within Veeva and Trial Master
Case Studies
At Vita Global Sciences, we’ve had the privilege of partnering with some of the most innovative names in the pharmaceutical industry. Our case studies showcase the breadth of our work, highlighting key projects that have revolutionized drug lifecycle development. From early-stage research to market-ready solutions, we invite you to explore these success stories that underscore our commitment to excellence and innovation.
