Cleaning Validation

Published: 9-Jan-2012

19 - 20 April 2012
Budapest, Hungary

In the manufacture of medicinal products and APIs, the cleaning of facilities and equipment is an important measure to avoid contamination and cross contamination. In compliance with the GMP regulations, cleaning is performed and documented according to the described procedures. In the past, cleaning effectiveness was often monitored only visually. However, residuals of APIs and excipients as well as of detergents are increasingly an issue in inspections and audits. The success of cleaning procedures has to be validated. This conference will discuss many questions relative to cleaning validation

Organiser: Concept Heidelberg

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