How do you evaluate the environmental and safety impact of your cleaning agent selection and disposal?
Cleaning validation is a critical process to ensure the quality and safety of pharmaceutical products. It involves verifying that the equipment and facilities used for manufacturing are free of any residues, contaminants, or microorganisms that could compromise the integrity or efficacy of the next batch. One of the key aspects of cleaning validation is choosing the right cleaning agent and disposing of it properly. How do you evaluate the environmental and safety impact of your cleaning agent selection and disposal? Here are some factors to consider: