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FDA Announces The Discontinuation Of Certain COVID-19-Related Guidance Documents - Operational Impacts and Strategy

In the wake of the Department of Health and Human Services' (HHS) February announcement that they will be discontinuing the COVID-19 public health emergency (PHE) declaration on May 11, 2023.

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The Long (Un)Winding Road: FDA Maps Out How The End Of The Public Health Emergency Will Impact Its COVID-19 Policies - Operational Impacts and Strategy

Since the beginning of the COVID-19 pandemic, the US Food and Drug Administration (FDA or the Agency) has issued more than 80 guidance documents describing flexibilities that would be available.

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Litigation Risks in FDA Remote Interactive Evaluations | Dechert LLP

Key Takeaways - The COVID-19 pandemic led the U.S. Food and Drug Administration (FDA) to pause most foreign and domestic inspections and begin conducting remote interactive.

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Wat gebeurt er wanneer je als machinist te maken krijgt met een (dodelijk) ongeval, zoals bij Boazum?

Wat gebeurt er wanneer je als machinist te maken krijgt met een (dodelijk) ongeval, zoals bij Boazum?
lc.nl - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from lc.nl Daily Mail and Mail on Sunday newspapers.

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FDAnews Announces FDA Drug GMP Facility Inspections During the Pandemic Webinar March 10, 2021

FDAnews Announces FDA Drug GMP Facility Inspections During the Pandemic Webinar March 10, 2021 PRWeb FacebookTwitterEmail FALLS CHURCH, Va. (PRWEB) February 24, 2021 FDA Drug GMP Facility Inspections During the Pandemic An FDAnews Webinar Has one’s inspection timeline been thrown for a loop because of COVID-19? How exactly will sites move forward with the FDA? The FDA restarted inspections last summer under a new guidance and during this webinar FDA inspections expert Kalah Auchincloss will share how assessments are proceeding and what criteria the FDA is using to determine which sites are inspected. Through Auchincloss’ experienced perspective, gain insights into how to prepare for an on-site inspection, from extended records requests to appropriate personnel access. We’ll also consider how the FDA is deciding on remote inspections and ways to equip your team for this method of assessment.

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