PQMS is a modular pharma QMS suite for cleaning validation, digital process management, and analytics—designed to ensure full pharmaceutical compliance
QMS Pro by Quascenta is an easy to use cloud-based quality management system that streamlines nonconformance, CAPA & change control processes. It empowers organizations to drive continuous improvement by providing a centralized platform for documenting NCs, investigating root causes, and implementing effective actions seamlessly. With powerful analytics and audit-ready documentation, QMS Pro helps you maintain compliance effortlessly
eProcess Pro by Quascenta is a game-changing, intelligent, lifecycle-based guided process validation platform that understands and speaks your language. It empowers consistent product excellence by seamlessly managing design, manufacturing, and safety, ensuring compliance and instilling confidence in your pharmaceutical initiatives
eResidue Pro by Quascenta can assist you in maintaining a compliant cleaning validation programme. The software seamlessly integrates all the cleaning validation data under a single umbrella thereby improving not only productivity but also acts as an aid in better decision making from the integrated data available on demand
Quascenta e Log Pro is a operator friendly software solution that revolutionizes the way pharmaceutical facilities manage essential GMP activities. By replacing traditional paper-based log records with a streamlined digital platform, logbook management system this eLog Pro enables efficient data capture, immediate analysis, and effortless compliance
ValDocPro by Quascenta is a game-changing qualification and document management software that goes beyond traditional document storage solutions. With its comprehensive qualification document tracking capabilities and robust document management features, ValDocPro ensures compliance, efficiency, and seamless collaboration throughout the qualification process
https://www.pqms.com/products/valdoc-pro/
https://www.pqms.com/products/eprocess-pro/