GoVal delivers flexible, scalable solutions through our secure cloud validation platform and on-premise deployments. Our Paperless Validation Solutions, powered by a comprehensive Validation Lifecycle Management System (VLMS), are tailored to pharma, biotech, and medical device teams. By aligning with ISPE GAMP 5 best practices, GoVal helps you apply a risk-based approach to computerized system validation (CSV), ensuring compliance without unnecessary effort or cost.
Our solutions support a wide range of industries, including pharmaceuticals, biotechnology, medical devices, clinical research laboratories, contract manufacturing organizations (CMOs), nutraceuticals, and food & beverage companies. This enables teams to streamline validation, reduce compliance risk, demonstrate data integrity, and stay audit-ready for regulators worldwide.
Digital validation software automates and manages validation processes for equipment, computerized systems, and manufacturing procedures. It ensures compliance with global regulatory standards, improves quality, and streamlines documentation to enhance audit readiness and reduce manual effort.
GoVal’s platform is built on the ALCOA++ principles—recognized by regulators such as the FDA, EMA, and ISPE—which define best practices for maintaining data integrity in regulated environments. These principles ensure that all data is Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, Available, and Traceable throughout its lifecycle.
GoVal’s Validation Lifecycle Management System (VLMS) follows recognized industry frameworks such as ISPE GAMP 5, applying a risk-based approach to computerized system validation. This ensures regulatory compliance while minimizing unnecessary documentation and validation effort.
Yes. GoVal adheres to ISPE GAMP 5 guidelines and global regulatory requirements (FDA, EMA), ensuring that all validation and data recording activities are risk-based, transparent, and audit-ready. This supports compliance across GxP environments, including pharmaceuticals, medical devices, and biotechnology sectors.
GoVal provides secure cloud and on-premise deployments, paperless validation workflows, configurable templates, and flexible pricing. It delivers scalable, audit-ready solutions tailored to the compliance needs of pharma, biotech, and medical device organizations.
GoVal includes comprehensive audit trails, secure document access, and real-time reporting capabilities. These features help reduce compliance risk, demonstrate data integrity, and ensure organizations remain inspection-ready at all times.
GoVal simplifies digital adoption with intuitive interfaces, guided onboarding, and dedicated support. The transition helps organizations achieve higher efficiency, reduced human errors, and lower operational costs while improving overall validation quality.
GoVal serves a wide range of regulated and process-driven industries, including pharmaceuticals, biotechnology, medical devices, clinical research, manufacturing, nutraceuticals, and food & beverage sectors.
GoVal offers customized pricing based on user requirements, team size, and feature preferences. Plans are available for both standard and enterprise deployments to suit diverse business needs.
Yes. GoVal supports both on-premise and cloud environments and is built for seamless integration with existing infrastructure, ERP systems, and process automation tools—ensuring smooth data exchange and workflow continuity.
By continuously aligning with current best practices and maintaining robust audit trail and traceability features, GoVal enables teams to remain compliant and adapt swiftly to new or updated regulatory requirements.
Key considerations include:
Contact us for personalized quotes based on your specific requirements, user count, and feature needs. Custom pricing available for both Standard and Enterprise solutions.