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Lupin's Goa facility completes GMP inspection by PMDA, Japan

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Lupin announced the completion of the Good Manufacturing Practices (GMP) inspection of its Goa facility (Unit - I & II), by the Pharmaceutical and Medical Devices Agency (PMDA), Japan. The inspection was conducted between 24 September 2019 and 27 September 2019.

The PMDA inspection closed with no critical or major observations.

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First Published: Sep 30 2019 | 3:35 PM IST

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