Dr Reddy’s said on Friday that it has received six major observations from German drug regulator for its Duvvada formulation facility. The company also said renewal of its EU-GMP certification next year will be based on the regulator’s satisfaction of the company’s corrective and preventive action taken at the plant.
The latest jab is a part of the never-ending saga of regulatory compliance woes the company has been facing starting November 2015 when USFDA sent a warning letter. The company has lost almost half of its market value since then. The warning letter slowed down new approvals significantly, hitting the company sales.
Here is a timeline of Dr. Reddy’s regulatory problems and the movement in its stock price
Data infographic by Ritesh Presswala
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