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MicroConstants China Receives Endorsement of OECD GLP Compliance
Date:5/26/2011

s Endorsement, along with the CNAS accreditation achieved last year, demonstrates that our Beijing team is capable of conducting high quality contract research services equivalent to those provided by our San Diego bioanalytical laboratory," said Dr. Gilbert Lam, co-founder of MicroConstants China and president of MicroConstants, Inc. in San Diego, California. "This is a significant accomplishment and we are very proud of their progress."

About MicroConstants China Inc.

MicroConstants China Inc. is a Contract Research Organization (CRO) that was established in 2007 by the founder and president of MicroConstants, Inc., a bioanalytical and PK specialty CRO in San Diego, California with over a decade of GLP compliance history. Located in Beijing, MicroConstants China provides preclinical and clinical pharmacokinetic analysis and early stage clinical trial management services, including clinical site qualification, trial monitoring, data management, biostatistics, and clinical summary reports to pharmaceutical and biotech companies worldwide. Additionally, the CRO offers QA audit and drug development project management services for preclinical toxicology and pharmacology studies in China. Its bioanalytical laboratory is fully GLP-compliant with USFDA, OECD, Japan MHLW and China SFDA guidelines. For more information about MicroConstants China and the contract research services they provide, please visit http://www.microconstants.com/china.


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