Become an expert in Quality Management with the Quality Manager (ISO 13485) training from Kader
Quality management is a crucial aspect of any successful organization, especially in the medical devices industry. Do you want to learn how to set up, manage, and improve a quality management system in accordance with the ISO 13485 standard? Then the Quality Manager (ISO 13485) training from Kader Academy is exactly what you need. What does this training entail, who is it suitable for, and how can you sign up?
What does the Quality Manager training cover?
The Quality Manager (ISO 13485) training is specifically designed for professionals working in the medical devices industry or those looking to start a career in this field. During this training, you will learn everything about developing, managing, and improving a quality management system according to the international ISO 13485 standard. This standard helps manufacturers, suppliers, and distributors of medical devices meet regulatory requirements and customer needs.
Through realistic case studies, you will learn how to optimize quality processes to comply with strict laws and regulations. The training provides in-depth knowledge and practical skills in the following areas:
- Understanding the requirements of ISO 13485 and how to ensure the safety of your medical product.
- Implementing ISO 13485 within an organization.
- Drafting and maintaining technical documentation.
- Designing and conducting internal audits.
- Risk management.
- Working in compliance with European regulations, such as the Medical Device Regulation (MDR).
Who is the training suitable for?
This training is designed for professionals involved in or responsible for quality management in the medical devices industry. This includes:
- Quality managers, quality officers, and internal auditors.
- Managers and executives responsible for quality assurance within their organization.
- Engineers, project managers, and other professionals working in the medical devices industry.
No specific prior education is required, but some analytical skills and knowledge of ISO 13485 and MDR 2017/745 are recommended. Depending on the participants, the training may be conducted in English.
How and where can you follow the training?
The training is delivered by experienced trainers with expertise in quality management and the medical devices industry. The program consists of interactive sessions that combine theory and practical application.
The training lasts five days and is available through in-person sessions at one of our training locations. The next training will begin on Tuesday, September 23, 2025, at Kader Group in Zeist (NL). Upon request, we can also deliver the training (partially) on-site at your company.
Sign up today!
Would you like to elevate your knowledge and skills in quality management to the next level? Register for the training here. On our website, you’ll also find detailed information about the daily program and costs. Note that the training has a maximum of 15 participants.
By completing this training, you not only invest in your own career but also contribute to the quality and safety of medical devices. This is not only valuable for you but also for society as a whole. Don’t wait any longer—sign up today!
