Welcome to the seminars at the Johner Institute
With the seminars at the Johner Institute, you get first-hand knowledge. Knowledge proven in practice that you can implement directly in your company. Knowledge that will make your daily work easier. Knowledge that you will use to argue with experts on an equal footing.
Registration for the seminar CPMS - Certified Professional for Medical Software
If you have any further questions contact us directly .
PS: Would you like another appointment? Get in touch with us! Or consider an In-house seminar .
Seminar Overview
Our Trainings
CPMS
The seminar "Certified Professional for Medical Software" (CPMS) prepares you perfectly for the exam or certification. It deals with all issues such as legal bases, QM-system, IEC 62304 and software development, usability (usability file), medical computer science, risk management and ISO 14971.
Risk Management & ISO 14971
Starting with the basics of risk management and ending with advanced topics such as quantitative derivation of risk acceptance: This seminar teaches you all you need to know to perform medical device risk management not only compliant to ISO 14971 but also to prioritize not only your V&V activities.
Customised training for you and your employees exclusively. We adapt the seminars to your specific needs and to the level of Knowledge of your team. We guarantee absolute confidentiality and a tailor-made seminar for you.
This two day training will enable the participants to plan and perform internal audits, write value adding and compliant audit reports and follow up audit findings effectively. On the first day we learn all about requirements and best practices of internal audits, and on day two the participants put theory into practice and perform a real internal audit by auditing the instructor. We do three internal audits with feedback sessions, so everybody gets a turn. Focus of this training is on auditing techniques not on the requirements, so this training enables you to audit against any regulations.
PRRC
MDR 2017/745 and IVDR 2017/746 require in Article 15 that all manufacturers appoint a "person responsible for regulatory compliance" from 26.05.2020 (MDR) resp. from 26.05.2022 (IVDR). In this seminar we address the requirements in detail and present best practices for implementation. We cover liability, internal/ external PRRC, joint responsibility, how to handle conflicts and required expertise.
Get in touch
Do you have any questions or would you like to give us feedback? We look forward to hearing from you!
Back To Top
Privacy settings
We use cookies on our website. Some of them are essential, while others help us improve this website and your experience.