How to Manage the Medical Device Product Development Lifecycle
There's no room for risk in medical device development. Patient safety — and the reputation of the developer — is at stake.
That's why complying with government regulations is a must. ISO 14971 specifies how to manage risk in medical device development. And IEC 62304 includes requirements for medical device software development.
Expose risk in medical device development.
Download this white paper to learn how to:
- Assess and control safety risks.
- Manage the relationship between requirements and risks.
- Trace risk and risk requirements across development.
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