Vita Global Sciences provides a wide range of validation services within the biopharma and life sciences industry. We bring our expertise of the pharmaceutical, biotechnology, and medical device business processes to ensure a practical, scalable approach to your validation requirements.
Process, Software & Equipment
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Protocol Writing (IQ/OQ/PQ)
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Validation Master Plan (VMP)
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Comissioning/Decomissioning
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Re-qualification
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Remediation
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FAT / SAT
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Cleaning (SIP/CIP)
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Aseptic
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Manufacturing Equipment
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Laboratory Equipment
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Utilities/HVAC
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Packaging & Labeling Equipment
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Concurrent
Process Validation
Process validation has many hurdles and challenges. Our experts have in-the-field expertise and can alleviate any concerns and help make your projects less daunting. We have the expertise and know-how to write your protocols as well as execute and finalize any and all reporting.
Software
VGS can assist with validation of quality, production and R&D software applications, and computer systems to comply with 21CFR part 11.
Equipment
Equipment can be as unique as the product to be manufactured. With our OJT experts, no matter how specific or tailor-made your equipment is, we can provide validation services that are both cost and time effective. We work with you and your teams to customize to the Master Validation Plan that suits your business/budget needs while maintaining the gold standard needed to meet your compliance needs.
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.
