Process Validation in Pharmaceutical

Process Validation in Pharmaceutical Process validation is defined by the FDA as the gathering and assessment of data from the process design stage through commercial production that produces scientific proof that a process is capable of reliably providing a quality product. The 3 stages of process validation are 1) Process Design, 2) Process Qualification, and 3) Continued Process Verification. In 2011, the FDA released Guidance for Industry Process Validation: General Principles and Practices Top 10 interview questions for pharmaceutical validation https://tech-publish.com/top-10-interview-questions-for-pharmaceutical-validation/