drug safety regulations

Drug safety regulations are rules set by government agencies to ensure that medications and treatments are safe and effective for public use. These regulations involve rigorous testing during the drug development process, including laboratory studies and clinical trials with human participants. Before a drug can be sold, it must undergo thorough evaluations to assess its benefits and risks. Once approved, ongoing monitoring is required to track any side effects or issues that may arise. The goal is to protect patients and maintain trust in the healthcare system by ensuring that only safe, effective drugs reach the market.