This workshop provides a comprehensive insight into the various subfields of cleanroom qualification – from regulatory requirements to the execution of individual tests.

Brief description:

The GMP- and standards-compliant manufacturing of pharmaceuticals depends on many influencing factors. The manufacturing process and thus the quality of the produced medicinal product are significantly affected by the environmental conditions prevailing during production. The qualification of ventilation systems and cleanrooms is an important component of the quality assurance concept for manufacturers in the life sciences sector.

This workshop offers a comprehensive overview of the different areas of cleanroom qualification – from regulatory requirements to the execution of individual tests. A particular highlight is the extensive practical component, which provides you with a realistic feel for cleanroom measurement technology. For this purpose, Testo Industrial Services operates its own ISO 7 cleanroom for practical exercises. Here, the learned skills can be directly applied in practice.

The seminar concludes with a certificate of completion.

Target audience and seminar objectives:

This practical workshop is aimed at all those who deal with cleanrooms or cleanroom qualification due to the regulatory environment. You will gain insights into the various measurement techniques used in cleanroom qualification – from regulatory requirements to the practical execution of individual tests – and after the seminar, you will know what is important for proper qualification. Particularly recommended for:

– Responsible personnel in production
– Purchasing
– Service companies
– Employees in quality assurance/QA/qualification

Our seminar speakers:

We offer you the best possible service through our many years of experience. Each individual is an expert in their field and shares their technical knowledge and experience during our seminars with you.