Workshop Overview
This two-day course offers a comprehensive exploration of essential cleaning methods vital for maintaining contamination control in the production of regulated medical and health products. Participants will gain insights into the principles of cleaning, emphasizing the removal of undesirable contaminant residues like viable bacteria or non-viable chemical particles. The course will cover various techniques such as Clean-in-place (CIP), ultrasonics, and sterilization, distinguishing between removal and deactivation methods crucial for rendering residues non-active. Special focus will be placed on regulatory requirements related to "Cleaning Validation" to prevent batch-to-batch contamination, a key concern during regulatory scrutiny. Additionally, attendees will learn to evaluate and optimize cleaning processes in accordance with industry standards and regulatory expectations, ensuring compliance while fostering continuous improvement and lifecycle management.