Many years of experience show that the current limit values for feed water and condensate lead to premature wear of system technology and medical devices, which jeopardises hygiene requirements and patient protection. Our seminars on sterile processing offer comprehensive training for employees and managers in AEMP and building services. The focus is on process water treatment, equipment technology and instrument knowledge, which are crucial for quality assurance and process optimisation.
The seminars cover measures for recognising and eliminating cost-intensive process risks as well as detailed limit values for water hardness, silicate content and conductivity in demineralised process water. Compliance with these limit values prevents surface changes to medical products and devices. Continuous monitoring of the necessary parameters improves the quality of the demineralised process water, which optimises the result of the reprocessing process and thus extends the service life of medical devices and equipment.

Another focus is on instrument science, which provides participants with a sound understanding of instruments and materials in order to minimise process risks. The seminars also offer insights into sterile goods logistics, legal certainty in the reprocessing of medical devices, decision-making and risk management for managers in the healthcare sector. Topics such as supply and disposal logistics, supply routes and interim storage are covered in order to develop efficient and hygienic logistics processes.
In addition, the seminar series increases the participants' decision-making confidence by helping them to analyse the liability risk in accordance with the Medical Devices Act. This enables them to make informed decisions about reprocessing processes. The seminars promote dialogue between colleagues and help to ensure that the AEMP meets the highest quality standards and guarantees maximum patient safety.