Sunday November 22 2009 | Biotechnology feed | All feeds
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Calvert Laboratories, Inc.
Download detailed PDF Members: We excel in the design and submission of preclinical development programs to various regulatory agencies (FDA, EPA, EEC, OECD, MHW) located all over the world. We are experienced in virtually all classes of compounds. We offer capabilities in the performance of studies to support the safety evaluation of drugs, chemicals and some devices from not only the discovery phase but through the preclinical phase up to the IND including first into man studies. We also perform studies supportive of the NDA.
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