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FDA Awards Precision Antibody Contract to Develop Monoclonal Antibodies for Influenza Vaccine Potency Assays
Date:10/19/2011

and always a potential bottleneck in influenza vaccine production," said Dr. Falko Schmeisser. "It is extremely important that additional approaches for reagent development be available, particularly in the event of an emerging pandemic influenza virus like the H1N1 in 2009."  Dr. Jun Hayashi, V.P. of Precision Antibody, said "we are honored to be selected and excited to be working with the FDA to develop these important antibodies. We are looking forward to initiating and growing this working relationship with Dr. Schmeisser's group."

About the Contract

This project HHSF223201110981P is supported with federal funds provided by the United States Food and Drug Administration (FDA). The content of this press release does not necessarily reflect the views or policies of the FDA, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. government.

About Precision Antibody (www.precisionantibody.com)

Precision Antibody provides customized, high-affinity monoclonal antibodies to pharmaceutical and biotechnology companies as well as to academic, government, and nonprofit research institutions for use in discovery, research, and testing of novel pharmaceuticals, biomarkers, and diagnostic tests. Precision Antibody is a one-stop service for antibody development, characterization (affinity determination by Biacore analysis), purification/production (from pilot to large scale), and conjugation, as well as stable cell line development, humanization, and hybridoma cell banking. Precision Antibody is a wholly owned service division of A&G Pharmaceutical, Inc. (www.agpharma.com) and is based in Columbia, MD.

Media Contact: Michael Keefe Precision, Antibody, 410-884-4100, mkeefe@precisionantibody.com

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