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Pharmaron Earns CFDA GLP Certification for Toxicology Facility
[March 03, 2014]

Pharmaron Earns CFDA GLP Certification for Toxicology Facility

BEIJING --(Business Wire)--

Pharmaron announced today that the company's GLP toxicology facilities in Beijing have earned a certificate of full GLP compliance from the Chinese Food and Drug Administration (CFDA) based upon a thorough inspection of its facilities, operating procedures and technical competency of the staff. Pharmaron is currently under contract with Sponsors wishing to file INDs in China as the result of this news.

"This certification by the CFDA is a reflection of Pharmaron's commitment to fully comply with the CFDA's GLP standards. It provides another avenue for our Sponsors to submit regulatory data from our facilities. Pharmaron is well positioned today to provide toxicology and regulatory expertise to our customers intending to include the China market in their drug development strategy," commented Pharmaron Chairman and CEO, Dr. Boliang Lou.

About Pharmaron

Pharmaron is a premier R&D service provider for the pharmaceutical and biotech industries. Founded in 2003, Pharmaron invests in its people and facilities enabling the Company to provide high quality R&D service across a number of disciplines, including chemistry, biology, DMPK, pharmacology, safety assessment, chemical and pharmaceutical development.

Pharmaron is steadily growing to meet the needs of its partners. With more than 2,000 employees and operations in China and the U.S., Pharmaron delivers superior scientific services while maintaining close communication with partners.

Pharmaron's mission is to provide the highest quality drug R&D services, helping our partners advance their projects in a timely and cost effective manner. More information is available at

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