
2nd Aseptic BioPharma Processing Summit
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About the event
Staying updated on regulatory requirements is crucial for ensuring compliance and maintaining the highest quality standards in drug manufacturing. The new EU GMP Annex 1 is officially published and will take effect in August 2023. How to deal with new challenges, adopt new methods aligning with stricter standards and embrace new innovative technologies? Our 2nd edition of the Aseptic BioPharma Processing Summit features comprehensive coverage on the implementation and management of the latest knowledge in aseptic, barrier, containment, and aseptic best practice technologies along with environmental monitoring systems, facility cleaning and disinfectant qualification, cleanroom operations, filtration, sterilization, and aseptic process simulation or media fill. This two-day summit encompasses expert insight into the robust aseptic processing requirements facing the industry as well as delving into more focus on the ever-growing rise of advanced therapies from allogenic cell therapies to innovative fill-finish lines. Come and join us in Vienna this November 9-10 together with manufacturers, regulators, and experts for the industry’s collective knowledge, gain different perspectives, and foster innovation in aseptic pharmaceutical manufacturing.

Conference learning points
- Overview of new EU GMP Guidelines and Annex 1
- Cleanroom design and environmental monitoring
- Optimization of fill finish operations
- Novel technologies for rapid sterilization and
decontamination - Automation and robotics in pharmaceutical production
- Single-use systems in aseptic manufacturing
- New developments in lyophilization and automatic
vial loading/unloading - Developing a holistic aseptic training program
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Sponsors
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