European Medicines Agency (EMA) Guidelines

The European Medicines Agency (EMA) Guidelines are a set of rules and standards designed to ensure that medicines approved in Europe are safe, effective, and of high quality. They provide developers and manufacturers with clear instructions on how to conduct research, test new medicines, and share data with regulators. By following these guidelines, the EMA helps protect public health and maintain trust in pharmaceutical products across Europe. Essentially, they are a roadmap that promotes consistent, thorough evaluation processes for new medicines before they reach patients.