Vita Global Sciences has expert programmers in the areas of SAS, R, and Python who tactfully and efficiently handle clinical trial data to provide automated outputs in accordance with industry and regulatory standards. Our team quickly adapts client specific technologies and best practices and provides insightful analysis and clinical study reports that empowers clients to draw interpretations and make well-informed decisions. A clearly laid out QC procedure helps us to deliver results on time, and with utmost quality.
Our Statistical Programming Capabilities Include
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Tables, Listings, and Figures
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Legacy to CDISC Conversion
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Support for Clinical Study Reports
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Support for Data Monitoring Committee reporting
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Integrated Summary of Safety and Efficacy (ISS/ISE)
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Support for post-marketing Periodic Safety Update Reporting (PSUR)
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Health Economics and Outcomes Research (HEOR)
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‘SEND’ - gene therapy
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FDA, EMEA, PMDA
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BIMO - clinsite datasets
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DSUR & PBRER (Periodic Benefit-Risk Evaluation Report)
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Investigational Brochure
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DMC (Data Monitoring Committee)
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Development Safety Update Report (DSUR)
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Real World Evidence (RWE)
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Automation
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Efficiency
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SDTM & ADaM
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Ad Hoc programming support
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Patient Profiles
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Specialty Expertise
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SAS, R, Python
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Automation & Efficiency
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Supporting Regulatory Adcom Meetings
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.
