Ranbaxy falsified drug data

The generic drug giant Ranbaxy falsified data on shelf life and efficacy on products made in their Paonta Sahib plant in India, the FDA said in a press conference today (Feb.26). In response, the FDA has invoked a regulatory action called the Application Integrity Policy (AIP). Until the company complies with the FDA, the "FDA will stop all scientific review of pending applications at Paonta Sahib, and no new applications will be reviewed," said Doug Throckmorton, a supervisory medical office