WASHINGTON, D.C. – Dr. Rajiv Shah, Administrator of the U.S. Agency for International Development (USAID), released the following statement regarding commitments received from vaccine manufacturers to reduce the prices of life-saving vaccines. The most transformative technology at our

WASHINGTON, D.C. – Dr. Rajiv Shah, Administrator of the U.S. Agency for International Development (USAID), released the following statement regarding commitments received from vaccine manufacturers to reduce the prices of life-saving vaccines. The most transformative technology at our

WASHINGTON, D.C. – Dr. Rajiv Shah, Administrator of the U.S. Agency for International Development (USAID), released the following statement regarding commitments received from vaccine manufacturers to reduce the prices of life-saving vaccines. The most transformative technology at our

The U.S. Food and Drug Administration today is announcing the approval of Merck’s redesigned drug container labels that include a new standardized format to improve readability and provide better information on product and strength differentiation. Merck’s Label Standardization Project

The U.S. Food and Drug Administration today is announcing the approval of Merck’s redesigned drug container labels that include a new standardized format to improve readability and provide better information on product and strength differentiation. Merck’s Label Standardization Project

The U.S. Food and Drug Administration today is announcing the approval of Merck’s redesigned drug container labels that include a new standardized format to improve readability and provide better information on product and strength differentiation. Merck’s Label Standardization Project

The U.S. Food and Drug Administration today cleared the Siemens Biograph mMR system, the first device to simultaneously perform a positron emission tomography scan, commonly known as PET scan, and a magnetic resonance imaging (MRI) scan. PET scans allow physicians to see how the organs and

he U.S. Food and Drug Administration today released draft guidance to provide regulated industries with greater certainty about the use of nanotechnology, which generally involves materials made up of particles that are one billionth of a meter in size. The guidance outlines the agency’s view

The U.S. Food and Drug Administration today announced that Alpharma, a subsidiary of Pfizer Inc., will voluntarily suspend U.S. sales of the animal drug 3-Nitro (Roxarsone), a product used by poultry producers since the 1940s. The move follows a recent FDA study of 100 broiler chickens that

U.S. Marshals, at the request of the U.S. Food and Drug Administration, today seized probiotic products from UAS Laboratories, Inc., of Eden Prairie, Minn. because the company markets the products as drugs. The seized products include DDS Acidophilus, DDS Plus, Probioplus DDS, DDS Junior, and