Validated disinfection, proven confidence
Disinfection in cleanrooms isn’t just about using the right products. It’s about proving they work, every time. Validation isn’t optional, but a regulatory requirement outlined in EU GMP Annex 1. That’s why we partnered with Ecolab to put our DOTCH® wipes and mops to the test in a EN16615 study, adapted for real-world pharmaceutical conditions.
Our newest article, “The value of validated cleanroom disinfection,” we explore how chemical efficacy meets mechanical performance to deliver proven contamination control. With tested effectiveness on surfaces like stainless steel and vinyl, and against organisms like Staphylococcus epidermidis and Bacillus subtilis, this study equips you with real data to support your disinfection validation.
Here’s what you’ll discover inside:
- Why dual-action cleaning is key to effective contamination removal
- How the EN16615 method was adapted for pharmaceutical cleanroom realities
- What this means for your validation process, compliance timeline, and peace of mind
We’re not just offering guidance. We’re empowering you to elevate your cleanroom cleaning practices with scientific precision and practical know-how. Because consistent technique means fewer risks and greater confidence in your contamination control.
If you have any questions still left, they will gladly be answered by our Customer Care team!