The matrix linking user needs, design inputs, risk controls, design outputs, verification and validation, so that every requirement and every risk control can be followed to its evidence.
Record or register Work product in the Medical electronics and medical device chips lifecycle
It is how the company shows design controls and risk management are complete. Gaps such as an unverified risk control or an unvalidated user need stay invisible until an auditor or regulator finds them.
The full lifecycle detail, with its charts, flows, tables and every section, is for registered members. Registration is free and takes a minute. You come back to this page afterwards.