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	Hoth Therapeutics Announces Production of HT-001 for Cancer Treatment Hoth Therapeutics, Inc. a biopharmaceutical company, today announced that it has signed a production agreement for both GLP and GMP materials associated with HT-001 ... Jan 01
	OraSure Technologies Provides Update on Its Emergency Use Authorization Application for Its Lab-based Oral Fluid SARS-CoV-2 Antibody Test The OraSure SARS-CoV-2 Antibody ELISA is intended for the qualitative detection of total antibodies to SARS-CoV-2 in human oral fluid specimens ... Dec 22
	APhA Statement Following Emergency Use Authorization of the Moderna COVID-19 Vaccine Statement from Scott J. Knoer, MS, PharmD, FASHP, executive vice president and CEO of the American Pharmacists Association, upon the Food and Drug Administration's (... Dec 19
	Coronavirus (COVID-19) Update: FDA Issues New Authorization for the BinaxNOW COVID-19 Ag Card Home Test Today, the U.S. Food and Drug Administration issued a new emergency use authorization (EUA) for the BinaxNOW COVID-19 Ag Card Home Test which ... Dec 17
	FDA Approves Y-mAbsâ€™ DANYELZAÂ® (naxitamab-gqgk) for the Treatment of Neuroblastoma Y-mAbs Therapeutics today announced that the U.S. Food and Drug Administration (â€œFDAâ€) has approved DANYELZA (naxitamab-gqgk) for the Treatment of Neuroblastoma.... Nov 26
	FDA grants priority review for avalglucosidase alfa, a potential new therapy for Pompe disease. The U.S. Food and Drug Administration (FDA) has accepted for priority review the Biologics License Application (BLA) for avalglucosidase alfa for long-term enzyme ... Nov 20
	North America Allergy Immunotherapies Market to Forecast to 2027- COVID-19 Impact and Analysis- By Treatment, Allergy type, Distribution Channel and Geography North America Allergy Immunotherapies Market to Forecast to 2027- COVID-19 Impact and Analysis- By Treatment, Allergy type, Distribution Channel and Geography... Oct 28
	Gilead's remdesivir gets U.S. FDA approval for hospitalized COVID-19 patients The U.S. Food and Drug Administration on Thursday approved Gilead Sciences Incâ€™s antiviral drug remdesivir for treating patients hospitalized with COVID-19... Oct 23
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Search Results

Hoth Therapeutics Announces Production of HT-001 for Cancer Treatment

OraSure Technologies Provides Update on Its Emergency Use Authorization Application for Its Lab-based Oral Fluid SARS-CoV-2 Antibody Test

APhA Statement Following Emergency Use Authorization of the Moderna COVID-19 Vaccine

Coronavirus (COVID-19) Update: FDA Issues New Authorization for the BinaxNOW COVID-19 Ag Card Home Test

FDA Approves Y-mAbsâ€™ DANYELZAÂ® (naxitamab-gqgk) for the Treatment of Neuroblastoma

FDA grants priority review for avalglucosidase alfa, a potential new therapy for Pompe disease.

North America Allergy Immunotherapies Market to Forecast to 2027- COVID-19 Impact and Analysis- By Treatment, Allergy type, Distribution Channel and Geography

Gilead's remdesivir gets U.S. FDA approval for hospitalized COVID-19 patients

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