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Patricia Van Arnum was executive editor of Pharmaceutical Technology.
January 02, 2008
Puerto Rico seeks to build its standing in biopharmaceutical manufacturing and research as it retains its role in bulk pharmaceutical and dosage manufacturing for small molecules.
Researchers and process chemists share approaches in synthesis of active ingredients and pharmaceutical intermediates.
December 28, 2007
The US Food and Drug Administration's joint panel of the Nonprescription Drugs Advisory Committee and the Endocrinologic and Metabolic Drugs Advisory Committee voted against recommending approval of the over-the-counter use of Merck & Co.'s “Mevacor” (lovastatin) 20 mg.
December 20, 2007
Merck & Co. initiated a voluntary recall of 11 lots of its Haemophilus influenzae type B vaccine, Pedvaxhib, and two lots of its combination Haemophilus influenzae type B/ hepatitis B vaccine, Comvax.
December 13, 2007
The US Food and Drug Administration issued a rule that clarifies its requirements for current good manufacturing practices for aseptic processing, water standards, and verifications standards.
December 06, 2007
The scientific demands on the US Food and Drug Administration far exceed its capacity to respond, according to a recent report by the Subcommittee on Science and Technology of the FDA Science Board.