Drug Registration

Drug registration is the official process where pharmaceutical companies submit detailed information about a new medication to government authorities to ensure its safety, effectiveness, and quality. The regulatory body reviews the data, including clinical trial results, manufacturing practices, and labeling, to determine if the drug can be legally sold and used by the public. Once approved, the drug receives a registration or approval certificate, allowing it to be marketed. This process helps protect public health by ensuring that medications meet strict standards before they reach consumers.