Tuttlingen – From production hygiene to sterile delivery to preparation: from June 15th to 17th, a triad of seminars will deal with various aspects of the cleanliness of medical devices, the normative specifications and practical action. The speaker is Klaus Frösel (Medical Device Services GmbH ).
The focus of the first seminar on June 15 is “Important aspects of medical devices delivered sterile”. The participants receive a complete overview of all aspects to be considered for sterile medical devices and - based on many examples - an insight into the technical background, including the topics of intended purpose, risk management, clean room, cleaning, packaging, sterilization and biocompatibility. “What does clean mean? How can I achieve clean medical devices? How do I ensure reproducible cleanliness in the long term?” Answers to these and other questions can be found in the seminar “Purity of Medical Devices: Production Hygiene, Product Cleaning and Monitoring”. After all, on June 17, everything revolves around the “processing of medical devices”. The very practice-oriented seminar provides information about legal requirements and current changes (including DIN EN ISO 17664 2nd/3rd edition and RDS 007), processing procedures and procedures, requirements for processing instructions and hygienic product design.
The seminar series at a glance:
06/15/2021: Important aspects of medical devices delivered sterile
06/16/2021: Cleanliness of medical devices: production hygiene, product cleaning and monitoring
06/17/2021: Processing of medical devices — DIN EN ISO 17664 (2nd/3rd edition), RDS 007
Please note that the seminars are only planned to be attended in Tuttlingen.
