Every Pharmaceutical and Biotech Organization aims to achieve excellent Quality Assurance throughout manufacturing, and to do this a Quality Management Solution (QMS) is essential, to manage SOPs, Methods, Work Instructions, and Specifications, as well as Deviations, CAPAs, Audits, Change Controls and Complaints. The QUMAS QMS ensures that quality standards are measured, maintained, analyzed, and trended for further improvement over time. This QMS provides Pharmaceutical and Biotech Organizations with the ability to feed information from one process to another, such as from a CAPA to a Change Control, creating an efficient and effective process environment and reducing duplication of effort, thereby reducing risk.
The QUMAS QMS automates record keeping and speeds up the release of drug batches, ensuring batch release is not held up by paperwork processing. Also, by providing high quality batches from a well-managed manufacturing process, the manufacturer can operate with the confidence that there will be less batch wastage and rework leading to higher margins and profitability for the organization. Brand and reputational risk is reduced, while process and quality improvements are significant.