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  • PMDA-CPE No.1116002: Procedure for Remote Inspection for Drugs & Regenerative Products
    Japan

    PMDA-CPE No.1116002: Procedure for Remote Inspection for Drugs & Regenerative Products

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  • FDA: Conduct of Clinical Trials of Medical Products During the COVID-19 Public Health Emergency
    USA

    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
    USA

    FDA: Post-marketing Adverse Event Reporting for Medical Products and Dietary Supplements During a Pandemic

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  • FDA : Enforcement Policy for Face Masks and Respirators During the Coronavirus Disease (COVID-19) (2020)
    USA

    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
    USA

    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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  • PMDA: Points to Consider for Reprocessed Single-use Medical Devices
    Japan

    PMDA: Points to Consider for Reprocessed Single-use Medical Devices

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