Biden administration still wants to ban menthol cigarettes, official says
The Food and Drug Administration's top tobacco official said Monday that the Biden administration is still pursuing its ...
Investopedia10d
Food and Drug Administration (FDA): What It Is and Does
Her expertise is in personal finance and investing, and real estate. The Food and Drug Administration (FDA) is a government agency that is responsible for the promotion and protection of public ...
Food Recalls Affect Millions of Americans in 2024
Millions of Americans are being impacted by food recalls every year as trust in food safety reaches a record low, according ...
Cherokee Phoenix5d
Nearly 2,000 drug plants are overdue for FDA checks after COVID delays, AP finds
Federal regulators responsible for the safety of the U.S. drug supply are still struggling to get back to where they were in ...
Roche's OCREVUS ZUNOVO Gets FDA Approval To Treat Relapsing And Progressive Multiple Sclerosis
Swiss drug major Roche (RHHBY) announced Monday that the United States Food and Drug Administration has approved OCREVUS ZUNOVO ...
Hopeful News for Users of One A.D.H.D. Drug
The D.E.A. is increasing its quota for the popular stimulant as patients still struggle to fill prescriptions.
The Jakarta Post8d
Strengthening Indonesia’s reputation in food and drug supervision
The Food and Drug Administration (BPOM) shoulders this critical responsibility, as outlined in Presidential Regulation No. 80/2017. The BPOM’s mandate extends beyond protecting domestic ...
5 takeaways from AP’s report on the big backlog of uninspected drug factories
Nearly five years after COVID-19, a new analysis by The Associated Press shows that U.S. regulators are struggling to address ...
Monthly Prescribing Reference7d
SC-Administration Ocrevus Zunovo Approved for Multiple Sclerosis
The Food and Drug Administration (FDA) has approved Ocrevus Zunovo ... “Ocrevus Zunovo gives patients and providers another option for receiving Ocrevus, building on a decade of robust safety and ...
Agios Announces FDA Orphan Drug Designation Granted to Tebapivat (AG-946) for Treatment of Myelodysplastic Syndromes (MDS)
Mitapivat, the company’s lead PK activator, was previously granted FDA orphan drug designation for the treatment of PK deficiency, thalassemia, and sickle cell disease. Tebapivat is not approved for ...
Alaska Dispatch News14d
Nearly 2,000 drug plants are overdue for FDA checks after COVID delays
The firms that are overdue for safety and quality inspections represent about 42% of the 4,700 plants that are currently ...