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Attend Virtually or in person to connect with IPS at the KENX Cleanroom Validation and Disinfection Conference 2022.

With the impending changes of Annex 1 as it applies the sterile environment and FDA’s Quality Consideration in Non-Sterile Drug Manufacturing Draft Guidance, the time has never been greater to ensure you have procedures mastered to comply with regulatory authorities. KENX’s hybrid conference showcases those paving the way in best practices in cleanroom qualification, disinfection, contamination control, environmental monitoring, and more. As a bonus, the event is co-located with Cleaning Validation and Critical Cleaning Processes and has over 40 tutorials to enhance your professional development.

Join KENX at the industry’s cleanroom validation event of the year! Whether you’re in QA, validation, or engineering; a novice or advanced professional; or, attending in-person or online, this is your chance to network with over 200 like-minded colleagues in the FDA-regulated environment.

For more information and to register click here.


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