Lupin clears Japanese regulator PMDA inspection of Goa facility
The Pharmaceutical and Medical Devices Agency (PMDA), Japan, has completed the Good Manufacturing Practice inspection of the company's Goa facility (unit I and II), Lupin said in a filing to the BSE.
New Delhi: Drug firm Lupin on Monday said Japanese regulator PMDA has closed inspection of its Goa facility with no critical or major observations.
The Pharmaceutical and Medical Devices Agency (PMDA), Japan, has completed the Good Manufacturing Practice inspection of the company's Goa facility (unit I and II), Lupin said in a filing to the BSE.
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The inspection was conducted between September 24 and 27, it added. "The PMDA inspection closed with no critical or major observations," Lupin said.
According to PMDA, its obligation is to protect the public health in Japan by assuring safety, efficacy and quality of pharmaceuticals and medical devices.
Based in Mumbai, Lupin is a player in the Cardiovascular, Diabetology, Asthma, Pediatric, CNS, Gl, Anti-Infective and NSAI D space and holds a global leadership position in the AntiTB segment.
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Farhat Nasim joined Medical Dialogue an Editor for the Business Section in 2017. She Covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She is a graduate of St.Xavier’s College Ranchi. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751 To know about our editorial team click here
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