« Previous
Next »
Titles
- Deciding when to submit a 510(k) for a software change to an existing device: guidance for industry and Food and Drug Administration staff1
- Electronic health information: CMS oversight of Medicare beneficiary data security needs improvement : report to Congressional requesters1
- FDA should further integrate its review of cybersecurity into the premarket review process for medical devices1
- Medical devices1
- States follow a common framework in responding to breaches of Medicaid data1
- Telemedicine in Mississippi: defining boundaries for a new frontier1