Process validation is the cornerstone of pharmaceutical manufacturing, a systematic endeavor to demonstrate that a production process consistently yields a product meeting its predetermined specifications. This episode provides a comprehensive overview of this crucial process and its associated regulatory landscape.

We delve into the key stages of process validation, from meticulously defining the process and crafting validation protocols to rigorous documentation and real-world testing. By examining guidelines such as CGMPs and highlighting practical examples, the discussion clarifies how regulatory expectations are met. This helps ensure that every batch of medication is both safe and effective.