Our event overview

How can Media Fill evaluation be automated efficiently while remaining GMP compliant?

This question is the focus of a joint comparative study conducted by Labor LS and Wilco AG.

We are pleased that our colleague Dr. Jessica Horn will present the study findings at the symposium. In her presentation, she will provide insights into the study approach, highlight the key findings, and discuss the potential of modern technologies for automated Media Fill evaluation in alignment with the requirements of EU GMP Annex 1.

Visit us at Booth 5. We look forward to insightful discussions with you.

Further information about Swiss Cleanroom Symposium can be found here.

From gowning to microbial control, how safe is your cleanroom really?

At NZW-Sommer in Berlin, our colleague Beatrix Gehlert together with Jörg Mesenich (Dastex Group GmbH), will present practical insights through live demonstrations, highlighting what truly matters in cleanroom garments, employee qualification in line with Annex 1, and safe gowning procedures. Drawing on real-world examples and lessons learned, they will uncover common weaknesses and share practical solutions that can be implemented directly.

Agenda: 

• Herstellung Reinraumbekleidung/Reinraumwäscherei
• Reinraumbekleidungssystem/Prozess
• Anforderungen Annex 1 Mitarbeiterqualifizierung
• Festlegung Punkte und Durchführung Mitarbeiterqualifizierung
• Ankleideprozedere Demo und praktisches Abklatschen
• Keimidentifizierung und Lösungsvorschläge
• Lesson learned and watch out
   

Find more information about the event here.

From gowning to microbial control, how safe is your cleanroom really?

At Aspetikon in Mannheim, our colleague Beatrix Gehlert together with Jörg Mesenich (Dastex Group GmbH), will present practical insights through live demonstrations, highlighting what truly matters in cleanroom garments, employee qualification in line with Annex 1, and safe gowning procedures. Drawing on real-world examples and lessons learned, they will uncover common weaknesses and share practical solutions that can be implemented directly.

Agenda: 

• Herstellung Reinraumbekleidung/Reinraumwäscherei
• Reinraumbekleidungssystem/Prozess
• Anforderungen Annex 1 Mitarbeiterqualifizierung
• Festlegung Punkte und Durchführung Mitarbeiterqualifizierung
• Ankleideprozedere Demo und praktisches Abklatschen
• Keimidentifizierung und Lösungsvorschläge
• Lesson learned and watch out
   

You are also welcome to visit us at booth 11.

Find more information about the event here.

What matters most when conducting sterility tests in practice?

At Aseptikon in Mannheim, our expert Olivia Halamoda will explain how to properly plan sterility tests and perform them under aseptic conditions. She will explore the interplay between method selection and qualified personnel and use case studies to demonstrate which approaches have proven effective in practice.

Agenda:

• Methodenwahl in der Sterilprüfung
• Anforderungen an aseptisches Arbeiten
• Personalqualifizierung
• Case Studies
   

You are also welcome to visit us at booth 11.

Find more information about the event here.

When results fall outside of specifications – do you know where to start?

From November 10 to 12, 2026, the Microbiology Compliance Manager Seminar will take place at NH Hotel Collection Heidelberg, where our colleague Frank Kugler will provide practical insights into the detection of critical microorganisms and the identification of contaminants in OOS results. In addition, our colleague Sandra Räder will shed light on the requirements and challenges related to sterility testing and the handling of OOS results in this sensitive area.

Nachweis kritischer Mikroorganismen & Keimidentifizierung bei OOS-Resultaten 
Frank Kugler

Prüfung auf Sterilität & OOS bei Sterilitätsprüfungen
Sandra Räder

Find more information about the event here.

How can the Monocyte Activation Test (MAT) be further optimized for robustness, efficiency, and cost-effectiveness? At PharmaLab, our expert Dr. Fabian Nürnberger will present insights from recent comparative studies and discuss opportunities for optimization.

Agenda:

• Evaluation of test robustness in comparison to traditional ELISA based MAT kits
• Comparative studies on reactivity of rapid MAT kits to different contaminants
• Can number of wells per test solution be reduced due to low well-to-well variation to make the MAT more cost and time efficient?

Visit us at Booth 42. We look forward to insightful discussions with you.

Further information about PharmaLab can be found here.