Quality management system as part of GMP
Quality management is a broad concept and includes maintaining the overview and control over the various activities within an organisation. Due to a rock-solid quality system management, pharmaceutical companies consistently achieve the desired product quality. In practice, this requires a quality management system, a formal entity within which all processes and procedures are documented and standardised.
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“Medicine manufacturers are required to maintain a QMS, as part of Good Manufacturing Practices (GMP). Traditionally, a quality management system consisted of paper-based documents, but as the digitisation increases, the process is now digital in most companies.”Sara - Business Manager
Quality management system - Advipro @ your service
- Developing and writing procedures, work instructions & related documents according to your requirements - our technical writers translate current GMP regulations into a well-functioning quality management system
- Optimisation of existing quality systems
- Validation & implementation of various digital QMS packages
- Operational support in executing your quality processes, such as monitoring deviations, CAPAs and change controls
Advipro has its own ISO9001:2015-certified quality system, under which all our testing and validation activities are carried out.
