Pharmaceuticals – Quality from the start
The efficient manufacturing of pharmaceuticals requires a continuous improvement and optimization of the existing processes and plants. As is required for the installation of new plants, these improvements and optimizations have to be carried out according to the current Good Manufacturing Practices (cGMP).
Whether for the erection of a new plant or the modification of an existing plant: We provide our GMP consulting services for engineering and automation projects in the pharmaceutical industry.
The path to achieving GMP compliance, i.e. establishing evidence that a plant or system is suitable for its intended purpose, begins during the design phase.
Our services contribute to:
a reduction of costs for obtaining and maintaining GMP compliance
an early detection of potential risks and mistakes
the implementation of effective processes for change control and configuration management
an increase in cost efficiency as a result of efficient planning and absolute adherence to the predetermined time schedule
a high quality documentation which is comprehensive and reliable and provides an excellent basis for audits by authorities