VALENCIA, Calif. and MELBOURNE, Australia, Aug. 11, 2022 AVITA Medical, Inc. , a regenerative medicine company that is developing and commercializing a technology platform that enables. | August 11, 2022
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Horizon scanning at the MHRA leads to a proposed new framework to enable the supply and increase in the availability of innovative new medicinal products made at the point of care to patients.
The Food and Drug Administration (FDA) yesterday banned the sale and importation of Flowflex COVID-19 rapid test kits, after 2.37 million flawed kits, allegedly made in China, entered the Taiwanese market and were sold to 13 government agencies.
According to regulations, the kits should be manufactured in factories in the US, but the importer allegedly imported poor-quality kits from China illegally and sold them as US-made products, FDA section chief Fu Ying-hsien (傅映先) said.
The FDA ordered that all Flowflex COVID-19 Antigen Home Tests that were imported by Safeway OA Supply Co Ltd (大鑫資訊) be recalled and warned customers against buying or