Medicines Standards

Medicines standards refer to the set of rules and quality criteria that ensure medicines are safe, effective, and of consistent quality. These standards cover everything from how medicines are manufactured, stored, and tested, to how they are labeled and packaged. They are established by health authorities and organizations to protect patients and healthcare providers, ensuring that every medicine on the market meets strict quality requirements, reduces risks, and performs as expected. In short, medicines standards help safeguard public health by maintaining high benchmarks for medicine quality worldwide.