Establishing compliance in production facilities and premises in a GMP environment is a prerequisite for successful market approval and marketing of products. We can manage your project or assist you with coordinating your quality systems and the qualification master plan from URS to design, supplier contacts to DQ, with installation to IQ and with commissioning of systems to OQ or PQ respectively. The necessary project documentation is created and supplemented throughout the entire process, including proofs as well as methodological analyses and safety-related clarifications.
In this way we support the creation of the relevant qualification, validation and compliance documents as well as the standard operating procedures in the form of SOP templates.
We coordinate the planning, realisation and implementation of regulated projects, including process monitoring and control. This enables us to contribute to an appropriate risk management and to implementing your projects in a calculable way.
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Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry’s standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged. It was popularised in the 1960s with the release of Letraset sheets containing Lorem Ipsum passages, and more recently with desktop publishing software like Aldus PageMaker including versions of Lorem Ipsum.
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