Good Manufacturing Practice (GMP) in the context of pharmaceuticals refers to a set of regulations, guidelines, and principles that ensure the consistent production of pharmaceutical products, including Active Pharmaceutical Ingredients (APIs), to the required quality standards. GMP ensures that medicines are manufactured in a controlled environment, following strict procedures to minimise the risks of contamination, errors, and deviations. See also Good Distribution Practices (GDP).
See also:
Relevant Legislation:
- UK Good Manufacturing Practice (UK GMP) – Ensures APIs are manufactured to the highest standards of quality and safety, reflecting EU guidelines before Brexit.
- EU GMP Guidelines – The European Union’s Good Manufacturing Practice guidelines provide detailed rules for API manufacturing, including the supply chain and distribution.
