The review of prescription and non-prescription drugs authorized is a long and intricate process, from research and development to clinical trial to ending up on the shelves of local pharmacies. Often, due to a variety of reasons, many drugs do not make it to market, and fail to be approved for public use. Here are some aspects of the regulatory process students interested in regulatory affairs should know. Therapeutic Value and Product Effectiveness The effectiveness of a drug allows it to pass clinical trials. Its success relies upon its therapeutic value, or how efficient the drug is at treating the.. READ MORE »
Students pursuing regulatory affairs careers should become familiar with the FDA and EMA, two international agencies that play a crucial role in drug approval.
