The year 2026 has seen a massive surge in the adoption of Single-Use Systems (SUS), posing a direct challenge to traditional cleaning validation. In 2026, many biopharmaceutical firms are swapping out stainless steel tanks for disposable bioreactors and tubing, which can reduce cleaning times by up to 80%. This 2026 trend is particularly popular for small-batch "personalized medicines" where...
Pharmaceutical cleaning validation is a mandatory and critical process within the industry, forming a cornerstone of Good Manufacturing Practices (GMP). Its core objective is to provide documented evidence, with a high degree of assurance, that a specific cleaning procedure consistently removes residues of the previous product, cleaning agents, and microbial contaminants to predetermined,...
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