Good manufacturing practice (GMP) describes the minimum standard that a medicines manufacturer must meet in their production processes. The European Medicines Agency (EMA) coordinates inspections to verify compliance with these standards and plays a key role in harmonising GMP activities at European Union (EU) level.

#Quality Management GMP vs. cGMP: What are the differences? By Marina Hoyos Published Jun 08, 2022 Updated Feb 08, 2023 GMP stands for “good manufacturing practices.” Life Sciences companies need to be GMP-certified in order to produce and sell their products. But what do GMP guidelines entail?