GoVal: Paperless Validation
To achieve GxP compliance, companies must implement a robust CSV program that includes validation planning, testing, and documentation. By doing so, they can reduce the risk of non-compliance and ensure that their products meet industry standards for safety and efficacy. A comprehensive CSV program also helps companies to identify and address issues early in the development process, reducing the risk of costly delays or recalls down the line. In short, CSV is an essential tool for ensuring the quality and safety of Life Sciences products and maintaining compliance with regulatory requirements.
GoVal is a comprehensive validation software solution designed to help Life Sciences organizations achieve GxP compliance by implementing automated, paperless validation systems. With GoVal, businesses can streamline their document storage and retrieval processes in a controlled and secured environment, reducing manual effort and cost. Say goodbye to the hassle of paper-based document handling and hello to a smarter, more efficient validation solution with GoVal.
Mastering Validation : Your Ultimate Guide
Create a comprehensive Master Validation Plan with GoVal to identify validation strategies, testing requirements, and GxP systems to be validated. Streamline your validation process today.
Defining User Requirements with GoVal
Define User Requirements (URS) and Functional Specifications (FS) with ease using GoVal's mapping and customization features. Streamline your validation process and achieve GxP compliance effortlessly.
Simplified GxP Assessment Process
GoVal's GxP assessment tool simplifies compliance by determining system GAMP category and suggesting required processes and documents for validation in the Life Sciences industry.
Risk-Based Validation Made Easy
GoVal enables risk-based validation for GxP computerized systems by allowing testing strategies based on severity and probability of occurrence of functional requirements and processes.
Streamlined Validation Workflow
GoVal's workflow automation simplifies the validation process with efficient document review and approval via electronic signatures, improving compliance and efficiency in the Life Sciences industry.
Automated Vendor Assessments
GoVal automates the vendor assessment process with electronic questionnaires sent to prospective vendors and feedback received, simplifying the process for Life Sciences organizations.
GxP Test Protocol Implementation
GoVal simplifies GxP compliance through risk-based validation, utilizing testing strategies based on severity and probability of functional requirement and process occurrence for computerized systems.
Requirement Traceability Matrix Generation
GoVal auto-generates a Requirement Traceability Matrix with test cases, risks, requirements, and discrepancy details for failed tests related to User Requirements Specifications (URS), streamlining the validation process.
Automated Compliance Reporting
GoVal simplifies regulatory compliance by generating reports such as Validation Summary Report, System Release Certificate, and Part 11 compliance certificate with a single click from Project Data.
