Glossary

Process Validation

Demonstrating that a process, within set parameters, can effectively and reproducibly produce product meeting its specification and quality attributes.

Details

Process validation demonstrates, from process design through continued verification, that the commercial process reproducibly achieves the predetermined quality attributes. Inspections cite batches that are not representative, worst case conditions and process variability not evaluated, and no trend monitoring after PPQ. Look at process design knowledge, the PPQ protocol and batch data, statistical trends, deviations and changes, and the continued process verification report.

Related sections

Related terms

Real inspection findings

Findings from regulators' inspection documents in which this term appears.

  1. Your firm lacked an adequate process validation program and sufficient validation studies for your drug product…
    FDA · FDA Warning Letter · 2023-09-05
  2. Lack of Process Validation You failed to provide data to demonstrate that you adequately validate your manufacturing…
    FDA · FDA Warning Letter · 2023-08-01
  3. You lacked process validation data to demonstrate you have adequately validated your manufacturing processes used to manufacture your OTC drug products and to demonstrate your processes are reproducible and…
    FDA · FDA Warning Letter · 2025-10-07
See 107 findings that mention this term

Source

WHO TRS 1019 Annex 3, GMP guidelines on validation, Glossary, Process validation