In the manufacturing of medicines, maintaining strict cleanroom behaviours is absolutely critical due to the highly sensitive nature of the process and the importance of ensuring patient safety. Cleanroom and GMP (Good Manufacturing Practice) behaviours are essential for safeguarding product quality, ensuring efficacy, and meeting regulatory compliance standards.

Adhering to cleanroom and GMP practices is fundamental to producing high-quality, safe, and effective products while maintaining compliance and operational efficiency. Without these practices, the risks of contamination and failure are significantly increased, which could compromise the safety and efficacy of medicines, ultimately putting patient health at risk.