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Efficient cleaning validation in the pharmaceutical industry

One basic GMP requirement is that the cleaning processes of equipment and facilities relevant to quality have to be validated. Both national and international authorities require this. Whereas in the past, the operator himself always had to set his hand to it, competent service providers are now available.

Clear strategy …

Chemgineering Technology Designers support you in the entire cleaning validation process. In close coordination with production and operating personnel, we develop your strategy. In so doing, you profit from our experience from numerous projects and our comprehensive knowledge of regulatory requirements.

… unfolds in clean implementation

In this approach we focus on the following activities
• Support in developing a validation strategy
• Support in developing the cleaning program:
processes, worst case scenarios, lead substances, limiting values
• Preparing the validation plans
• Conducting the tests
• Documentation of the tests and drafting the validation reports

Read more in our Newsletter No. 62 (Nov. 2011)

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