GoVal - Validation Life Cycle Management System (VLMS)

The GoVal Validation Lifecycle Management System (VLMS) is a digital validation solution designed for pharmaceutical and life sciences companies. According to the vendor, it aims to provide an efficient and compliant paperless validation process to meet global regulatory requirements. The software is suitable for small, medium, and large businesses operating in the pharmaceutical and life sciences industries. It is commonly used by professionals such as Quality Assurance Specialists, Validation Specialists, Compliance Officers, Regulatory Affairs Professionals, and Pharmaceutical Manufacturers.

Key Features

Computer System Validation (CSV): According to the vendor, the software allows users to perform GxP Assessments, define Validation deliverables, and generate documents electronically with an automated workflow and electronic signature.

Process Validation: The vendor states that users can define User Requirements, conduct risk assessments, execute test cases, and generate reports to ensure efficient process validation.

Equipment Qualification: According to the vendor, the software enables users to define User Requirements, perform risk assessments, execute test cases, and generate reports for equipment qualification in compliance with regulatory standards.

Cleanroom Validation: The vendor claims that users can define User Requirements, perform risk assessments, execute test cases, and generate reports to validate cleanroom environments.

Method Validation: According to the vendor, users can define User Requirements, conduct risk assessments, execute test cases, and generate reports for accurate and reliable method validation.

QMS Framework: The vendor states that the software allows users to establish a comprehensive Quality Management System (QMS) framework by defining User Requirements, conducting risk assessments, executing test cases, and generating reports.