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By Kent Mansfield , president TruTag Technologies, Inc.
Published April 1, 2015
As the global problem of counterfeit and diverted drugs continues to grow worldwide, will our medicine soon carry secure identifiers woven into the very fabric of the drug product? Advancing technology is finally allowing drug makers the ability to implement on-dose authentication. Read More »
By Julie Kuriakose , UPM Pharmaceuticals
Published May 1, 2014
Comparing manufacturing methods for one immediate-release low-dose form, we found that dry blend needed less equipment and was more “QbD-ready” than wet granulation or geometric dilution. Read More »
Published July 28, 2010
EMD Serono’s NDA for Cladribine Tablets has accepted for filing as a therapy for relapsing forms of multiple sclerosis (MS). Read More »
Published January 2, 2007
Ranbaxy Laboratories has received approval from the FDA to manufacture and market Atenolol Tablets USP, 25 mg, 50 mg, and 100 mg. The Office of Generic Drugs, U.S. FDA, has determined the Ranbaxy formulations to be bioequivalent and have the same the… Read More »
By Michelle Calhoun, Director of Sales and Marketing, Commercial Operations
AbbVie, world leader in pharmaceuticals, provides Contract Manufacturing Services that span API manufacturing, biologics, potent drugs, finishing and packaging of pharmaceutical drug products. Our vast network of global manufacturing facilities allow… Read More »