The ACR-368-tailored OncoSignature assay is being used to identify patients most likely to respond to the company's lead drug candidate ACR-368 in an ongoing, registrational-intent, phase IIb trial in ...

Acrivon Therapeutics (ACRV) announced the U.S. Food and Drug Administration, FDA, has granted Breakthrough Device designation, BDD, for the ...

Former health secretary Janette Garin, who was involved in the Dengvaxia vaccine anomaly, said the Department of Justice's ...

THE Food and Drug Administration (FDA) warned the public on Friday, January 24, 2025, about the presence of an unregistered ...

SSL certificates are vital for verifying your website authenticity to visitors and ensuring secure connections. Having no active SSL certificate (or one that doesn't have the level of trust you ...

The website also displays a registration certificate, purportedly issued by the Philippine Food and Drug Administration (FDA), with the registration number FR-4000011793485. As of writing ...

It is mandatory for a person undertaking reverse charge transactions to register for GST. Reverse-charge mechanism is a provision where the liability of tax is on the receiver of goods, and not the ...

The FDA says that food companies will have until Jan. 15, 2027 to stop using the dye. Drugmakers will have an extra year, until January 2028, to comply with the change. Red 3, also known as ...

Red Dye No. 3, or erythrosine, is a synthetic red food dye once popular in candies and cakes. The ... [+] FDA bans Red Dye No. 3 under the Delaney Clause, citing cancer risks observed in lab ...

After intense lobbying on the part of affected industry stakeholders for approval of the African swine flu vaccine, the Food and Drug Administration has finally but “conditionally” issued “a two-year ...

Officials cited a statute known as the Delaney Clause, which requires FDA to ban any additive found to cause cancer in people or animals. The dye is known as erythrosine, FD&C Red No. 3 or Red 3. The ...