FDA threatens Dr Reddy’s with US import ban
26 Nov 2015
The US Food and Drug Administration, which had issued a warning letter to Dr Reddy's Laboratories over quality issues (See: FDA seeks third-party audit of all Dr Reddy's plants), has said it might withhold approval of the company's fresh drugs and stop imports if no corrective action is taken.
The regulator said it had found several violations with regard to current good manufacturing practices (CGMP) at three of its plants.
"At Dr Reddy's Laboratories' facilities, we identified significant deviations from CGMP for manufacturing of active pharmaceutical ingredients (APIs) ... we found significant violations of CGMP regulations for finished pharmaceuticals," US FDA noted.
"FDA strongly recommends that you evaluate global manufacturing operations to ensure compliance with CGMP regulations and requirements, comprehensively and immediately," the regulator said in its letter dated 5 November addressed to DRL chairman Satish Reddy.
"Until you complete all corrections and FDA confirms your compliance with CGMP, FDA may withhold approval of any new applications or supplements listing your firm as a drug product or API manufacturer," it said.
Earlier this month, the country's second-largest drug maker received a warning letter from the US drug regulator relating to two of its API manufacturing plants and a formulation plant in Andhra Pradesh and Telangana.
In response to the letter, DRL chief executive G V Prasad had said the company is in the process of shifting some of the products from these plants to other facilities and considering third party assessment for its plants. However, FDA was "not satisfied" with the reply.
The US agency asked the drug maker to provide a comprehensive evaluation of the extent of inaccuracies in recorded and reported data and include a detailed action plan to fully investigate the scale and root causes of "deficient documentation and data management practices".
