How to write unambiguous design and development inputs and meet ISO 13485 requirements

Struggling to create a clear and consistent requirements engineering document? You're not alone, BHH member Scilife's got you! Requirements engineering is a crucial element in the development of medical devices that align with user needs, market demands, and regulatory standards.

To guide you in mastering this key skill, Scilife's delighted to invite you to their upcoming training session "How to write unambiguous design and development inputs and meet ISO 13485 requirements" with Peter Sebelius, CEO and Founder of Medical Device HQ.

Here's what you'll learn:

• Avoid common mistakes in requirements engineering using real-world examples.
• Streamline development by understanding the importance of effective categorization of requirements.
• Ensure consistency, clarity, and completeness in documentation through practical application of patterns.
• Discover the significance of making design and development inputs complete, unambiguous, verifiable, and conflict-free.

This training session, scheduled for February 8th at 15 hrs is free, all you need to do is register using this link.

Scilife is excited to have you on board for this informative training session. Upon completion, you'll receive a digital certificate of attendance!

Register now HERE.