This thread is for discussing the lifecycle document "Design Inputs & Hazard Analysis: stage guide".
How user needs become design input requirements that are complete, unambiguous and verifiable, how essential performance and basic safety are defined, and how the first hazard analysis and use specification are written, so a design review can approve the inputs. For systems engineers, risk management leads, usability engineers and regulatory affairs leads.
Read the document: https://www.thesemiconhub.com/lifecycle/medical/med-design-inputs/document
Point out anything that is wrong, unclear or missing, and say which section you mean. Reviewers read this thread when they audit the document.