Cleaning validation and contamination control in the pharmaceutical industry

The article examines how cleaning validation is evolving towards more digital and traceable environments, incorporating technologies such as TOC, rapid microbiological methods and recombinant endotoxin reagents. It explains the role of data integrity, instrument qualification and the use of appropriate consumables in ensuring analytical reliability. It also highlights the transition to RMM, the modernisation of BET testing and the importance of an integrated contamination control strategy aligned with cGMP and Annex 1.

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