The Food and Drug Administration Dec. 4 issued guidance on how to conduct clinical trials for medical products during the COVID-19 public health emergency. FDA said the guidance provides general considerations to assist trial sponsors in assuring participants’ safety, maintaining compliance with good clinical practices and minimizing risks to trial integrity.

The agency also on Dec. 4 issued an enforcement policy for mammography quality standards during COVID-19. The enforcement policy provides general considerations to facilities that, because of COVID-19, may have temporarily ceased performing mammography or that may be continuing to perform mammography while facing difficulty in complying with certain quality standards requirements during the public health emergency.

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The Centers for Disease Control and Prevention Feb. 19 released a report on the low use of COVID-19 antiviral drugs among individuals age 65 and older, a…
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The Food and Drug Administration today released two guidance documents; one related to low-risk wellness products (including certain wearable devices) and the…
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The Centers for Disease Control and Prevention Dec. 11 released a report that found last year’s version of the COVID-19 vaccine was 76% effective in preventing…
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The AHA provided recommendations to the Food and Drug Administration Dec. 1 in response to a request for information on the measurement and evaluation of…
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The Food and Drug Administration has identified a Class I recall of Baxter Life2000 Ventilation Systems due to a cybersecurity issue discovered through…
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The Food and Drug Administration yesterday published an announcement from Otsuka ICU Medical saying that the company issued a voluntary recall for a mislabeled…