Monday, August 10, 2020

FDA

FDA Reissues Emergency Use Authorizations Regarding Respirators

Due to the available respirator shortages, these revised recommendations are essential.

FDA Authorizes First Next Generation Sequencing Test For Diagnosing COVID-19

Using next-generation sequencing tools means that the test can generate information about the genomic sequence of the virus present in a sample. 

FDA Issues Guidance On Prescription Drug Marketing Act

The relevance of this modification affects health care providers, patients affected by COVID-19 and related conditions, and the life science companies themselves.

FDA Publishes New Updates For Healthcare Professionals

The FDA staff, researchers, and partners are working virtually around the clock to keep medical professionals updated with the absolute latest information.

FDA Issues June 2020 Statistical Guidance Report, Available For Download

This latest document is a series of FDA guidance reports that are created to keep healthcare professionals informed on the latest in the COVID-19 public health emergency (PHE).

FDA Pursues Action Against Companies Offering Misleading Antibody Tests

The FDA issued advisory letters to three companies that have allegedly been promoting faux antibody tests for the treatment of COVID-19.

FDA Updates Document For Public Health Emergency Guidance

The guidance document was issued by the Center for Drug Evaluation and Research of the FDA and was intended for IRBs and clinical investigators.

FDA Steps Up In Ongoing Coronavirus Health Crisis

Here are the largest takeaways of the newest measures put in place by the FDA.

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