Sterilization of Medical Devices – Inhouse Training

qtec Academy | Sterilization of Medical Devices

Fundamentals, Common Practices, and Pitfalls in Practice

The sterilization of medical devices to protect human health is a central element in the development, manufacture, use, and reprocessing of medical devices. When applied correctly, it can ensure the safety of medical devices and improve product quality.

It is important to distinguish between products that are manufactured and sterilized under aseptic conditions and medical devices that are sterilized on-site by the user.

Gain an understanding of the validation process for sterilization procedures and learn the normative fundamentals according to DIN EN ISO 11135, DIN EN ISO 11137 and DIN EN ISO 17665.

Learn how to select appropriate methods, process parameters, and service providers; understand the tasks and responsibilities you have as a manufacturer, service provider, or testing laboratory; and discover how to maintain sterility over the long term.

Let's work together!

Individual sessions for this topic are not available for booking. However, we offer it as an in-house training course that is tailored specifically to your needs.

Get a quote now

Let's work together!

Individual sessions for this topic are not available for booking. However, we offer it as an in-house training course that is tailored specifically to your needs.

Get a quote now

Event Category

Inhouse Training

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You can book a free consultation session four weeks after attending the seminar: We will help you to put what you have learned into practice straight away and answer any questions you may have afterwards.

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