23—THURSDAY, Jan. 23, 2025 (HealthDay News) — The U.S. Food and Drug Administration ... to Sanofi stating that FDA inspectors found irregularities with the facility's bioreactor, the vessel ...
The U.S. Food and Drug Administration has ... a warning letter was sent to Sanofi stating that FDA inspectors found irregularities with the facility's bioreactor, the vessel used to grow organisms ...
THURSDAY, Jan. 23, 2025 (HealthDay News) -- The U.S. Food and Drug Administration ... sent to Sanofi stating that FDA inspectors found irregularities with the facility’s bioreactor, the vessel ...
The availability of drugs in public health facilities in Kano State has significantly ... the government’s efforts to sanitize the drug market by enforcing the utilization of the established ...
French pharmaceutical giant Sanofi has received a warning letter from the U.S. Food and Drug Administration following an inspection at its drug manufacturing facility in Framingham. French ...
Generic injectable-focused Gland Pharma has received establishment inspection report (EIR) from the U.S. Food and Drug Administration for its facility in Dundigal, near Hyderabad. The company has ...
The Food and Drug Administration is banning dye Red No. 3 in food and oral medicinal products. The substance gives a cherry-red hue to certain foods and medicines. The FDA ban comes on the cusp of ...
More than 100 people have used Ireland’s first medically supervised injecting facility (MSIF ... community safer by removing instances of drug-injecting from public spaces,” he said.
A recall of a Pinsarella Roman Pizza product from Pinsarella Food has been classified as a Class I recall by the U.S. Food and Drug Administration (FDA) due to undeclared wheat and soy. Newsweek ...
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