How to make your garment programme audit-ready by default

Under the revised EU GMP Annex 1, your cleanroom garment system is no longer just a workwear decision. It is a documented element of your Contamination Control Strategy. That means qualification, defined lifecycle limits, re-qualification studies, and evidence your inspectors can follow. Yet, many sites are still working from inherited assumptions rather than defensible data.

To help you close that gap, we're hosting a focused webinar bringing together our expertise as a cleanroom partner and an independent specialist presentation by Carsten Moschner (CMC3).

What we'll cover:

✔ What Annex 1 requires of cleanroom garments and why
✔ Risk management applied to garments: identification, assessment, and monitoring
✔ The new approach to qualification: Body-Box testing, end-of-life analysis and re-qualification studies
✔ Defining and documenting your garment system specification
✔ What inspectors actually look for and where gaps most commonly appear
✔ Site vs. supplier responsibilities and shared accountability