Life Sciences Collection
Access Life Sciences policy templates and content here
- Risk Management SOPManage cybersecurity risk associated with medical devices.
- Data Integrity Audit Report for Production Software as a Medical DeviceHow to run a data integrity audit for software as a medical device.
- Cybersecurity Governance SOPHow to establish and maintain cybersecurity governance for medical devices.
- Secure Design and Development SOPHow to integrate security practices into the design and development of medical devices.
- Third-Party Risk Management SOPHow to manage cybersecurity risks associated with third-party components.
- Secure Deployment and Configuration SOPHow to securely deploy and configure medical devices.
- Secure Disposal SOPHow to securely dispose of medical devices and associated data.
- Cybersecurity Testing and Validation SOPHow to test and validate cybersecurity measures in medical devices.
- Vulnerability Management SOPHow to manage vulnerabilities throughout the medical device lifecycle.
- Comprehensive Medical Device Cybersecurity Policy
- Software as a Medical Device Submission TemplatesHow to document an SRS submission to the FDA.
- Incident Response and Business Continuity SOPHow to respond to incidents and ensure business continuity for medical devices.
- Documentation and Maintenance SOPHow to develop and maintain cybersecurity documentation for medial devices.