Thank you for attending the webinar
We’ve prepared a 48-page eBook on requirements engineering and ISO 13485.
It’s a structured reference you can refer to after the webinar, and it includes the product requirements diagram Peter presented.
You’ll get the eBook for free when you subscribe to our newsletter.
Subscribers receive regular industry insights, course updates, and other free premium templates.
Feel free to share this page with colleagues or peers who might find the resources useful too.
Level up in design control and requirements engineering
If you want the full toolbox and practical guidance, we’d recommend the Requirements Engineering and Design Control courses by Peter.
Gain expertise in design control and be efficient in medical device product development with this self paced, interactive online course.
- Grasp the “big picture” of medical device development through design control.
- Learn to identify and avoid common pitfalls in product development.
- Communicate efficiently with your team, minimising frustration and confusion.
- Strengthen procedures and practices in design control.
- Ensure regulatory compliance and enhance product development efficiency.
Learn about writing medical device user needs and design input requirements in this self-paced, interactive online course.
Crafting clear and effective user needs and design inputs is a complex task, but it’s essential in successful medical device development. With a solid grasp of requirements, you can streamline the design process, saving valuable time and resources.
By the end of the course you will not only be able to write effective requirements, but also manage them throughout the project lifecycle.
We recommend that you take the design control course before this course unless you already have a good understanding of design control.