Cleaning Validation
Cleaning validation is required under Annex I of the EU GMP Guidelines for the Manufacture of Sterile Medicinal Products. According to these guidelines, cleaning procedures must be specified and their effectiveness validated. Cleaning validation is therefore an integral part of the contamination control strategy.
Effective cleaning in the manufacture and preparation of highly toxic substances is therefore essential. Due to changing conditions, technical innovations, and similar factors, cleaning procedures must be modified, revalidated, and reevaluated.
With our many years of expertise, we can assist you in validating your cleaning processes.
Whether you’re using different cleaning cloths, cleaning agents, or cleaning methods, we’ll work with you to determine the best overall solution.


