About VaultGxP
VaultGxP Solutions redefines what's possible by revolutionizing how organizations handle compliance, data management, and operational efficiency in highly regulated environments.
If paperless is your goal, Integrated Quality Management should be your strategy. Embrace automation and digital solutions to eliminate paper-based processes, reduce manual errors, and accelerate compliance while maintaining the highest standards of quality and regulatory adherence. With VaultGxP, you gain the efficiency of automation alongside the flexibility and security needed to thrive in today's regulated industries.
Our Solutions
Enables Realtime Tracking, Integrates seamlessly within a Quality Management System (QMS), offering enhanced capabilities to ensure compliance, efficiency, and data integrity in regulated environments.
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A complete digital Quality Management System automates processes and compliance for Deviation, Change Control, Out Of Specification, Laboratory Incidents, CAPA, Trend Analysis
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Smart Audit ensures compliance and quality in regulated industries, identifying risks, improving processes, and ensuring accountability by meeting regulatory and industry standards.
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Pharma consultancy services provide expert guidance on regulatory compliance, quality assurance, and market strategies to optimize pharmaceutical operations and ensure success.
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VaultGxP streamlines regulatory filing for life sciences, pharma, and devices, ensuring submissions to global bodies like FDA, EMA, and PMDA with efficiency and compliance.
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Our Process
We begin with an in-depth consultation to understand your specific needs and objectives.
Based on your requirements, we develop a customized testing plan tailored to your materials.
we offer follow-up consultations to review the results and discuss any
further steps.
Testimonials
“VaultGxP helps us efficiently manage and track over 200 complaints monthly and 1,000 annually, significantly enhancing our capacity to scale up operations and improve case handling.”
“VaultGxP’s expertise in QMS processes and digital platforms ensures lifecycle quality, manages audits, improves efficiency, and enhances our ability to consistently deliver excellent results.”
“Upgrading to VaultGxP’s digital platform improved quality, traceability, audit readiness, streamlined operations, and enhanced compliance and efficiency in audits.”
“VaultGxP software integrates seamlessly into operations, aligning quality management, enhancing efficiency, and ensuring consistent quality across all processes effortlessly.”
“VaultGxP’s reliability, smooth installation, user-friendly interface, and tracking capabilities enhance efficiency, quality management, compliance, audits, and organizational results.”
Sample Management involves all the activities during the lifecycle of a sample in the lab. Right from sample login to generation of certification.
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The VaultGxP Calibration and Preventive Maintenance (PM) Program offers a digital solution that enhances the management.
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The VaultGxP Stability Program within a digital system provides a comprehensive, streamlined solution for managing stability testing.
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In today’s fast-paced, highly regulated industries such as life sciences, healthcare, and manufacturing.
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Empower Your Training with E-Learn" is a powerful tagline or slogan for promoting an e-learning platform or solution.
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Deviation Management is an essential process within Quality Management Systems (QMS), particularly in regulated industries.
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Change Management is a critical process for any organization, particularly in dynamic industries like life sciences.
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In industries like pharmaceuticals, biotechnology, and other regulated sectors, ensuring that products meet quality.
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In laboratory environments, particularly in regulated industries such as pharmaceuticals, biotechnology.
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A Critical Tool for Continuous Improvement and Compliance Trend analysis in a Quality Management System (QMS).
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Smart Audit is a critical component of maintaining quality and compliance within regulated industries like pharmaceuticals.
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Laboratory layout design services focus on optimizing space utilization, workflow efficiency, and safety by integrating.
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We offer support in managing and updating essential documentation needed for medical industry regulatory compliance.
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GMPs provide a detailed roadmap for maintaining quality in drug production. These crucial guidelines dictate how manufacturers.
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These standards guide the establishment and functioning of Quality Management Systems (QMS) to ensure that products are safe.
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Warehouse Management Systems (WMS) optimize storage, tracking, and operations across multiple locations.
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VaultGxP streamlines regulatory filing, ensuring efficient, compliant submissions to global bodies like FDA, EMA, and PMDA.
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