Validation Management Systems (VMS) Software

Digitizing the validation life-cycle revolutionizes the speed, accuracy, intelligence, transparency and management of validation. Achieve quality assurance best practice, improve productivity and reduce time-to-market, changeover and cycle-times with Kneat paperless validation software.

Performing validation to Equipments maintaining the schedules are critical to the Pharma Industry in order to produce quality products as well as to meet the cGMP. Performing the validation without missing timeline for a single equipment within the its due date is a great challenge to the industry. To meet these requirements Pharma Soft Sol designed validation management software. Pharma Software Solutions is a software company aimed to develop the software specially to meet regulatory requirements in Pharma & Biotech Industry.

Novatek’s Validation Management software creates a roadmap for validation practices that goes beyond customer processes, and promotes unified data views across any organization. The system is designed for variety of processes some of which that include: Validations, Workload Forecasting, Sample Inventory, Sample Management, Control & Distribution, Testing of Validation Samples. This type of information is required for validation cost-to-serve analyses, which produce great insights into compliance, methodology and profitability.

Accelerate critical approval, verification, and compliance management processes while ensuring FDA compliance with Tricentis Vera. With Tricentis Vera, Digital Validation means more than just applying electronic signatures to shift traditional documents to a computer screen. It means modernizing the Computer Systems Validation process to shed cumbersome, extraneous documentation practices and enabling compliance to be achieved as a byproduct of good software quality practices.

Veeva Vault Validation Management is a digital solution that manages qualification and validation activities for computerized systems, facilities, utilities, equipment, and processes. The application tracks system inventory, requirements, and project deliverables. Validation professionals can create validation activities, execute test scripts digitally, and generate traceability and summary reports throughout all stages of the validation process. Validation Management is unified with Vault QualityDocs and Vault QMS to connect quality events and key artifacts.

OnShore developed and exclusively distributes ValidationMaster, a Lean Enterprise Validation Management and Quality System exclusively for life sciences companies and government agencies – and a platform to deliver AI/ML for validation. The proprietary software suite combines OnShore IP with best-of-breed technologies to deliver a robust solution for timesaving, cost-effective validation and verification of literally any enterprise system or process.

Xybion’s Validation Management software allows companies to create a unified process for creating, managing, and executing all validation activities across multiple sites and multiple countries and multiple regulatory guidelines as necessary. The essence of validation as required by the FDA is to provide documented evidence that provides a high degree of assurance that all processes, equipment, instruments, facilities, software, and materials used will consistently produce a product meeting its pre-determined specifications and quality attributes.

Validation Manager is a cloud-based software service that automates the verifications and validations of laboratory methods and instruments. Validation Manager is a software service that makes instrument and assay verifications and validations easy and efficient. Validation Manager use cases range from verifications and validations to routine quality control of the laboratory. Furthermore, test manufacturers can empower their customers to conduct faster verifications of their instruments, and even conduct troubleshooting activities remotely.

ValGenesis VLMS is an industry standard digital validation platform for life sciences worldwide. Peerless in capability, it empowers you to enforce standardization, ensure data integrity, reduce risk, lower the cost of quality, and strengthen your compliance posture.

With the FDA’s shift to Computer Software Assurance (CSA), AssurX has developed a risk based validation model that provides customized validation services based on a critical thinking approach that supports the GAMP 5 Model. CSA encourages automated testing as well as the acceptable use of vendor documentation and formal testing of the installed software. The new approach reduces the amount of redundant documentation and validation activities and increases the focus on ensuring the software works as intended in the installed environment.