In Sanofi’s case, the FDA had issued its certificate of product registration on December 22, 2015. Sanofi, however, failed to submit the necessary post-marketing authorization requirements after ...

MANILA, Philippines – The Food and Drug Administration (FDA) is set to hold the first summary hearing on the new rules of procedure for the certification of all contraceptive products on Monday ...

MANILA, Philippines — Two manufacturers of self-administered home test kits for COVID-19 have so far applied for special certification before the Food and Drug Administration (FDA), its acting ...

A team from the Philippines’ Food and Drug Administration is scheduled to fly to Russia next week to inspect the Sputnik V vaccine manufacturing plant of the Gamaleya Institute as part of regulatory ...