The FDA ensures the safety and effectiveness of generic drugs by rigorously reviewing and approving them. This process includes doing bioequivalence trials to compare the active ingredient’s performance in the generic drug and its brand-name version, adhering to region-specific regulatory requirements, conducting clinical trials, ensuring high-quality manufacturing, and continuously monitoring drug quality. Generic drug manufacturers can expedite the approval process by studying FDA guidelines early and regularly consulting with the FDA.
WordPress users targeted by devious new credit card skimmer malware
E-commerce websites running on WordPress are being targeted by cybercriminals who are inserting malicious JavaScript code to steal payment information, Sucuri cyber security researchers have
