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India’s Dr Reddy’s gets FDA warning on three drug plants

By Zeba Siddiqui MUMBAI (Reuters) – Dr Reddy’s Laboratories Ltd, India’s second-largest drugmaker by sales, said on Friday it has received a “warning letter” from the U.S. Food and Drug Administration over what the regulator has deemed inadequate quality control procedures at three manufacturing plants in southern India. The warning letter means Dr Reddy’s will not receive FDA approvals to sell drugs manufactured at the plants for now, a blow for business at a company which relies on the United States for a majority of its sales. The plants make a significant contribution to company sales, with one alone accounting for 10-12 percent, Dr Reddy’s said.

U.S. regulator sued for withholding information on GMO crops

A food safety advocacy group sued an arm of the U.S. Department of Agriculture on Tuesday, saying it illegally withheld public information on genetically engineered crops. The lawsuit, brought by the Center for Food Safety (CFS) against the USDA’s Animal and Plant Health Inspection Service (APHIS), claims the regulator has routinely failed to respond as required to requests for records that relate to many concerns with the GMO crops. The lawsuit accuses the agency of violating the Freedom of Information Act dozens of times, unlawfully withholding information for more than 13 years.