"FDA"

The Sinovac Covid-19 vaccine is safe to use despite not being listed on the World Health Organisation’s Emergency Use Listing (EUL), said Food and Drug Administration (FDA) secretary-general Dr Phaisan Dankhum.

Scribners Catskill Lodge in Hunter, N.Y., was one in a nationwide sea of hotel establishments to temporarily close last year when the pandemic wiped out tourism and travel.

WASHINGTON - The Food and Drug Administration cleared the first coronavirus vaccine for emergency use in children as young as 12 on Monday, expanding access to the Pfizer-BioNTech shot to adolescents before the next school year and marking another milestone in the nations battle with the virus.

The reason Russia’s Sputnik V vaccine has not been registered for use in Thailand is because the importer Kingen Biotech Ltd has not yet submitted full documentation for registration, the Food and Drug Administration (FDA) said on Friday.

The Food and Drug Administration (FDA) has so far approved three Covid-19 vaccines for use in Thailand, while three more companies are in the process of registration, FDA secretary-general Dr Phaisan Dankhum said on Monday.

Keeping aspirin tablets in the fridge can degrade the drug’s quality and even make it dangerous to consumers, the Thai Food and Drug Administration (FDA) has warned.

Three private firms have been given the okay to import and register for the administration of Covid-19 vaccines, while another company is under consideration, Dr Paisan Dankhum, secretary-general of the Thai Food and Drug Administration (FDA), said on Monday.

WASHINGTON - In the wake of a congressional report last month that found the presence of toxic metals at high levels in many baby foods, the Biden administration Friday announced the first steps aimed at reducing arsenic, lead and other toxins in baby and toddler products.

Johnson&Johnson has submitted all the documents required for the Thai Food and Drug Administration (FDA) to consider its adenovirus vaccine, FDA’s secretary-general Dr Paisan Dankhum said on Monday.

WASHINGTON - The Food and Drug Administration late Saturday granted emergency use authorization to Johnson & Johnson's single-dose coronavirus vaccine, providing the United States with a long-anticipated tool that adds firepower and flexibility to the nation's accelerating inoculation effort - but also presents new challenges.

WASHINGTON - The Food and Drug Administration said Friday evening that it will "rapidly work" to authorize the Johnson & Johnson single-shot coronavirus vaccine, shortly after an expert committee unanimously recommended the vaccine.

WASHINGTON - A third coronavirus vaccine could soon be available in the United States, a one-shot regimen made by pharmaceutical giant Johnson & Johnson that proved safe and effective in a clinical trial and completely protective against hospitalizations and deaths, according to a Food and Drug Administration review released Wednesday.