Photographs: Mark Blinch/Reuters
The Supreme Court on Friday issued notice to Centre and Ranbaxy Laboratories Ltd on a PIL seeking cancellation of the company's license and a CBI probe against it for allegedly supplying adulterated drugs in the country.
Agreeing to examine the allegations, a bench headed by Chief Justice P Sathasivam, however, refused to pass any interim order for restraining the company from manufacturing drugs.
"The matter requires consideration and we will examine it but we cannot grant any interim stay," the bench said.
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SC notice to Centre, Ranbaxy on plea for cancelling its licence
Image: The court passed the order on a PIL filed by advocate M L Sharma seeking action against the company for allegedly supplying sub standard and adulterated drugs.Photographs: Jo Yong hak/Reuters
The court passed the order on a PIL filed by advocate M L Sharma seeking action against the company for allegedly supplying sub standard and adulterated drugs.
Sharma had earlier also filed a similar petition which was dismissed by the apex court.
The court, however, had granted liberty to Sharma to file fresh petition with additional documents in support of his allegations.
In his PIL, Sharma alleged that "Ranbaxy was fined $500 million by the US Food and Drug Administration for making and selling adulterated drugs".
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SC notice to Centre, Ranbaxy on plea for cancelling its licence
Image: The case might make it difficult to induce professionals to join Boards of companies.Photographs: Ronen Zvulun/Reuters
The PIL also sought sealing of all its manufacturing units in New Delhi, including those in Paonta Sahib in Himachal Pradesh and Dewas in Madhya Pradesh.
He alleged that despite Ranbaxy pleading guilty to supplying adulterated drugs in the US and it being fined such a huge amount, the Centre has not taken any action to prohibit or ban the drugs made by the company.
He also sought action against Indian drug regulator, Central Drug Standards Control Organisation, for permitting Ranbaxy to sell drugs in India, especially in the wake of the results of the USFDA probe against the company.
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