Quantifying And Assessing Cleaning And Disinfection Residues: A Case Study

While cleaning and disinfectant residues can be viewed as evidence of effective cleaning, they can also pose contamination risks or signal a lack of control. This presentation explores the impact of these residues on ATMP cGMP manufacturing facilities. Driven by the latest Annex 1 revisions, we'll guide you through minimizing residues by strategic regime design.

Join David Collins (Ecolab) and Aoife Duffy (HiTech Health) as they delve into identifying, assessing, and addressing disinfectant residues and their associated risks. Gain practical insights into designing cleaning regimes that prioritize residue management. A comprehensive case study, presented from both the manufacturer and disinfectant supplier perspectives, will demonstrate residue assessment methodologies and data evaluation techniques that go beyond simple visual checks.

Key Takeaways:

• Align cleaning and disinfection processes with regulatory compliance.
• Identify and mitigate the risks of disinfectant residues.
• Design cleaning regimes that effectively manage residues.
• Understand residue assessment and data evaluation through a real-world case study.