CERTIFICATE COURSE – CONTENT
| Module 1 | General regulatory requirements for software for or as a medical device | 05.11.2026 |
| Module 2 | Implementation of IEC 62304 and IEC 82304-1 for medical device software manufacturers | 12.11.2026 |
| Module 3 | Risk management for medical device software – ISO 14971 | 19.11.2026 |
| Module 4 | UX and Usability for Medical Software and Apps – IEC 62366-1 | 01.12.2026 |
| Module 5 | Cybersecurity – IT security for medical devices | 11.12.2026 |
Single modules also available!
Course language: ENGLISH
PARTICIPANTS
- Medical device manufacturers whose products contain software or are software products in their own right, from the areas of regulatory affairs, quality management, systems and software engineering, usability engineering, requirements engineering, project management, risk management, product management, IT, management,
- Service provider / supplier in the medical technology,
- Consultants for medical software
- Newcomer & Start-Ups
COSTS
- Early bird (until October 08, 2026): Euro 2.350,- (excl. VAT)
- Standard (starting with October 09, 2026): Euro 2.590,- (excl. VAT)
- incl. seminar documents as PDF and a certificate of participation
- Installment payment on request!
- Apply for our scholarship – 2 x € 490,-!
DISCOUNTS
10% discount for
- Cluster members (Standortagentur Tirol, Forum Medtech Pharma, Human.technology Styria, LISAvienna, MTC Upper Austria, Innovation Salzburg, ecoplus NÖ, Bayern Innovativ)
- from the 2nd participant of a company/organization
- for returning visitors
- The discounts cannot be combined.
- All seminar discounts at a glance
LOCATION: ONLINE
All you need for the ONLINE modules is a laptop with camera and microphone. You will receive the course materials in PDF format and the link to the virtual classroom via email. Each module is designed to be interactive, similar to a face-to-face seminar: you can ask the instructor questions, there will be practice examples, and you will have the opportunity to interact with other participants.