The Novatek Quality Management Suite provides an improved and more complete solution for traditional Quality Management. Novatek’s Quality Management System (Nova-QMS) is a comprehensive tool for the management of quality processes in the Pharmaceutical and Life Science Industries. To enhance the capabilities, Nova-QMS further assures regulatory compliance across departments, by integrating our Calibration and Preventative Maintenance module (Nova-CPM) and our Validation Management system to include additional important components that contribute to a total quality process.
Calibration and Maintenance is no longer just an overhead expense. It plays a critical role in the success of capital intensive companies in a regulatory environment. The more an organization can maintain and optimize its asset management, the more it can compete in cost effectiveness, quality, delivery time, and new product innovations. Asset management in Regulatory…
Maintaining consistent product quality and quality processes can be challenging in today’s pharmaceutical manufacturing environments. Regulated industries such as the Pharmaceutical, Biotech and Life Sciences are required to maintain Good Manufacturing Practices (GMP) to meet regulatory requirements. Not only do you need to meet GMP requirements you must also be able to prove this to…
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…
