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HSPA: 3.0 CE Points
(certified until 3 Feb 2027)
10 Feb 2025
Event Details

RUMED Online Training Program:
The complexity of instrument reprocessing and related processes is increasing, requiring a deep understanding of correlations within various workflows. This expertise is crucial for making informed decisions and upholding the high quality standards in our daily work at RUMED. Achieving this requires a strong foundation of technical and procedural knowledge. To meet these demands, the RUMED Academy offers a comprehensive online training program consisting of two levels: 'Reprocessing Technician RUMED (Level I)' and 'Senior Processing Technician RUMED (Level II)'.

The modules are conducted in English, and delivered by experienced international experts with extensive knowledge and practical experience in the field of application in the operating room (OR) and instrument reprocessing. The content of the modules is based on the comprehensive DGSV and HSPA courses, ensuring a well-rounded and relevant training experience.

Reprocessing Technician RUMED (Level II):
The Level II program consists of 9 individual modules (see below “Module Overview”). The target group is RUMED managers, RUMED technicians and other employees in RUMED with proficient English/Spanish language skills and practical experience in a reprocessing structure for medical devices.

Module ​7.1: Quality Management and Validation II​:
The focus of this lesson is on creating a quality management manual, with standard operating procedures (SOPs), controlled documents, and how to create an flowchart. The basics of a quality management manual are presented, including its structure, content and importance for the organization. We deepen the understanding of how to create SOPs as controlled documents so that they are implemented effectively. The concept of a controlled document is explained and how to manage, monitor and update documents to ensure compliance with quality standards and guidelines. Finally, you will learn about risk assessment to identify, evaluate and develop appropriate risk reduction measures. 

Certification:
Upon successful completion of this module, a certificate with 3.0 CE points by the HSPA is issued as proof of achievement. Each module concludes with a knowledge quiz. Once you have completed all modules and provided the corresponding certificates to the RUMED Academy (contact@rumedacademy.com), you will be awarded the Reprocessing Technician RUMED (Level II) certificate.  

Participation Cost:
€ 80.00 per Module

Module Overview (Level II):
6.1 Structure and Design of RUMED and its Processes II
7.1 Quality Management and Validation II
7.2 Quality Management and Validation III
7.3. Quality Management and Validation IV
7.4 Quality Management and Validation V
8.2 RUMED Management III
8.3 RUMED Management IV
9.1 Material and Instrument Sciences II
11.1 Processing of Medical Devices in the Supply Chain II

Module Overview (Level I):
1.0 Standards, Laws and Regulation
2.0 Hygiene and Microbiology
3.0 Cleaning and Disinfection I
3.1 Cleaning and Disinfection II
4.0 Sterilization
5.0 Proper Machinery Working
6.0 Structure and Design of RUMED and its Processes
7.0 Quality Management and Validation I
8.0 RUMED Management I
8.1 RUMED Management II
9.0 Material and Instrument Sciences I
10.0 Packaging and Sterile Barrier Systems I
10.1 Packaging and Sterile Barrier Systems II
11.0 Processing of Medical Devices in the Supply Chain I

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Scientific Chair
Christina Lehmann
RecoTec-Software GmbH - Weilheim i. Obb., Germany​
Partners
Event Agenda
10.30 CET | PART 1
Welcome & Introduction
2 min
Quality Management in CSSD
10 min
SOP (Standard Operating Procedure)
8 min
Steps to Create a Bullet Point List
2 min
Structure of a SOP
2 min
Symbols of a Flowchart
3 min
Steps to Create a Flowchart
85 min
Key Takeaways
3 min
12.25 CET | BREAK
5 min
12.30 CET | PART 2
Why Risk Management?
2 min
Components of a Risk Management
10 min
Risk Assessment Tools
10 min
How to - Risk Assessment
34 min
Live Discussion - Voting, Q&A
2 min
Key Takeaways
2 min
GET CERTIFIED (INDIVIDUAL)
15 min
I Will Learn To
Basics of a quality management manual
The meaning of a controlled document
Learn how to create an SOP for a quality management manual
How to create a flowchart
Methods for risk assessment
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