Is the FDA Failing Women?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 750, doi. 10.1001/amajethics.2021.750
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- Publication type:
- Article
Works matching IS 23766980 AND DT 2021 AND VI 23 AND IP 9
Results: 13
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Who, If Not the FDA, Should Regulate Implantable Brain-Computer Interface Devices?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 745, doi. 10.1001/amajethics.2021.745
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- Publication type:
- Article
3
Recovery.
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 739, doi. 10.1001/amajethics.2021.739
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- Publication type:
- Article
4
How Pseudoscience Generated US Material and Device Regulations.
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 721, doi. 10.1001/amajethics.2021.721
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- Publication type:
- Article
5
FDA Device Oversight From 1906 to the Present.
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 712, doi. 10.1001/amajethics.2021.712
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- Publication type:
- Article
6
What Should Cardiac Patients Know About Device Cybersecurity Prior to Implantation?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 705, doi. 10.1001/amajethics.2021.705
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- Publication type:
- Article
7
AMA Code of Medical Ethics' Opinions Related to Implantable Devices.
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 702, doi. 10.1001/amajethics.2021.702
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- Publication type:
- Article
8
What Should the Public Know About Implantable Material and Device Innovation in the US?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 697, doi. 10.1001/amajethics.2021.697
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- Publication type:
- Article
9
What Should Patients Be Told About Device Representatives' Roles at the Point of Surgical Care?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 692, doi. 10.1001/amajethics.2021.692
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- Publication type:
- Article
10
What Should Physician-Researchers Tell Patient-Subjects About Their Relationships With Industry?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 685, doi. 10.1001/amajethics.2021.685
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- Publication type:
- Article
11
What Do Clinicians and Organizations Owe Patients With Recalled Implanted Devices or Materials?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 679, doi. 10.1001/amajethics.2021.679
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- Publication type:
- Article
12
How Should Clinicians and Organizations Assess Risks and Benefits of First-in-Human Implantation of Investigational Devices?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 673, doi. 10.1001/amajethics.2021.673
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- Publication type:
- Article
13
How Differently Should the FDA Regulate Drugs and Devices?
- Published in:
- AMA Journal of Ethics, 2021, v. 23, n. 9, p. 669, doi. 10.1001/amajethics.2021.669
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- Publication type:
- Article