Pharma, Biotech & Chemical Processing
The construction of biotechnology and pharmaceutical facilities places particular demands on all those involved. Our teams of engineers have proven their efficiency and ability in numerous projects. From the selection and procurement of plant components to the supervision of construction and assembly, you can rely on our experience and proactive involvement.
Competence in the Pharma, Biotech and Chemical Processing Industries
Our corporate structure enables us to offer our competencies worldwide. We exploit these synergies to develop innovative, cross-border solutions for the benefit of our customers in the Pharma, Biotech and Chemical Processing industries. That is how we network the competence of our experts for your success.
Your facility in compliance
Validation is the documented proof that a facility will repeatedly produce a product to the stated specifications. This includes compliance with EU and FDA guidelines (GMP requirements), identification of problems and their correction, assessment of risks and exploiting potential for optimisation to maximum advantages.
With our outstanding knowledge and experience, you can count on our assistance when it comes to the trouble-free processing of all validation work. Our validation master plan establishes the procedures and responsibilities - from design qualification and the compliance of the facility and equipment with operational documents and specifications as well as operational verification right up to the subsequent procedure qualification and process validation.
We always keep a close eye on the increasingly demanding requirements of the licensing and inspection authorities. We clearly record all qualification and validation work in writing. This is because first-class documentation is essential: it verifies the GMP compliant examination of the plant and processes conducted as part of an inspection.
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