Do you work with medical device software process design? Together with Intertek Academy, we offer a 2-day course covering medical device software process design based on IEC 62304. This course is designed for professionals developing or managing medical devices containing software or software as a medical device (SaMD).
📅 Next session: Stockholm, Sweden, 25-26 November 2026 (held in English)
Our upcoming course covering medical device software process design based on IEC 62304, in cooperation with Intertek Academy, provides knowledge on how to design a process for the development and maintenance of medical device software according to the IEC 62304 standard and the regulatory requirements that apply to medical device software.
This course covers:
-
Current software practices
-
Designing high-quality software in a regulated environment
-
Standards for regulatory compliance
-
Implementation examples for achieving compliance
-
Practical applications of the requirements of the 62304 standard
Who should attend?
Professionals involved in software development, risk assessment, QA, process improvements, or procurement of software components/subcontractors.
What you’ll learn
After the course, participants will have an understanding of how to employ design processes for medical device development based on the 62304 standard, in order to achieve regulatory compliance and how to design high quality software in a regulated environment.
The course is held in English and led by Maria Rickardsson, Senior Quality & Regulatory Affairs Consultant at Aurevia.
Questions? Contact: academy@aurevia.com
Learn more and register
Share this article
