Australia, U.K. Authorities Okay Ranbaxy’s Indian Plant

Ranbaxy Laboratories (Gurgaon, India) says that the U.K.’s Medicines and Healthcare products Regulatory Agency (MHRA; London) and Australia’s drug regulatory body Therapeutic Goods Administration (Canberra) have issued GMP certificates for Ranbaxy’s Paonta Sahib, India facility, following a joint audit conducted last October. MHRA’s approval will cover U.K. product filings and also apply to product filings for the entire European Union, Ranbaxy says. The U.S. FDA said last month that the Paonta Sahib facility falsified data and test...

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