News
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 ...
Rockville, Md., July 12, 2010 — In an effort that will contribute to raising the quality of medicines in the Philippines and surrounding regions, the Laboratory Services Division (LSD) of the ...
MANILA, Philippines — The Food and Drug Administration (FDA) is requiring the manufacturer of Reno brand liver spread to secure proper authorization for the product to be marketed in the country ...
MANILA, Philippines — Researchers in the country are looking into the possible use of saliva as a sample for coronavirus testing, the Department of Health said Wednesday. DOH Undersecretary ...
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