USA Medical Device
Showing all 10 results
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FDA : Enforcement Policy for Face Masks and Respirators During the Coronavirus Disease (COVID-19) (2020)
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FDA : Enforcement Policy for Ventilators and Accessories and Other Respiratory Devices During the Coronavirus Disease 2019 (COVID-19) Public Health Emergency
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FDA Guidance : Acceptance and Filing Review for PMAs
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FDA Guidance: 510(k)-Review-Program (2020)
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FDA Guidance: Annual Reports for Approved Premarket Approval Applications (PMA) (2019)
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FDA Guidance: Providing Regulatory Submissions for Medical Devices in Electronic Format (2020)
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FDA Guidance: Requests for Feedback and Meetings for Medical Device Submissions: The Q-Submission Program
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FDA Guidance: Types of Communication During the Review of Medical Device Submission (2014)
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FDA: Conduct of Clinical Trials of Medical Products During the COVID-19 Public Health Emergency
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FDA: Post-marketing Adverse Event Reporting for Medical Products and Dietary Supplements During a Pandemic
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