3rd Aseptic BioPharma Processing Summit

October 29-30, 2024
Vienna, Austria
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97Days 12Hours 31Minutes 47Seconds

ABOUT THE EVENT

In the wake of revised Annex 1 regulations coming into effect, what are the implications? How pharma manufacturers are setting new benchmarks for product manufacturing? What’s new about Contamination Control Strategy? The 3rd Aspetic Biopharma Processing conference will navigate the latest developments in aseptic processing, quality risk management, robotics and automation, microbial monitoring, automated visual inspection, etc. It will serve as a platform for sharing experiences on parenteral production, GMP practices, state-of-the-art facilities and machine design, quality assurance for audits, etc. This two-day summit encompasses expert insights into fill finish tech transfer challenges, aseptic process simulation (APS) validation and considerations, barriers technologies, lyophilization, innovativemodels for aseptic manufacturing, sealing and packaging technologies, PUPSIT, etc. It will be a full immersion in the latest regulatory updates, advancements in cleanroom technologies, strategies to detect and contain contamination, and approaches to empower the aseptic workforce. Additionally, sessions will cover the use of virtual reality for training and ensuring sterility assurance of products, providing attendees with practical knowledge and tools to enhance their manufacturing processes and comply with regulatory standards.

Join us at the 3rd Edition of the Aspetic Biopharma Processing Summit in Vienna, Austria this October 29-30 together with professionals from pharma production, manufacturing, engineering, quality control, quality assurance, regulatory bodies, new technology providers, etc. for the industry’s collective knowledge, gain different perspectives, and foster innovation.

CONFERENCE LEARNING POINTS

  • Ensuring CCS in Aseptic Environments
  • Quality assurance for audits
  • Empowering the aseptic workforce through training
  • State of art- Facility and Machinery design
  • Manual vs. Automated visual inspection
  • Overview of new EU GMP Guidelines and Annex 1
  • Cleanroom design and environmental monitoring
  • Novel technologies for rapid sterilization and decontamination
  • Optimization of fill finish operations
  • New developments in lyophilization and automatic vial loading/unloading

SPEAKERS

‎‎‎‎‏‏‎ ‎Yuan-An Liu

BioNTech SE

‏‏‎ ‎Andrew Gravett

AstraZeneca

‏‏‎ ‎Varadharaj Vijayakumar

WuXi Biologics

‏‏‎ ‎Jean-Rene Authelin

Sanofi

‏‏‎Stephanie Knueppel

Roche

Sune Klint Andersen

Janssen Pharmaceutical

‏‏‎ ‎Doris Lacej

Profarma

‏‏‎ ‎Sara De Pinto

Merck Group

‏‏‎ ‎Eva Ulied

Boehringer Ingelheim

‏‏‎ ‎Micheal Quinn

Ardmac Group

‏‏‎ ‎Ilaria Lo Presti

GSK

‏‏‎ ‎Beatriz Roques

Reig Jofre

Stephan Heck

BIPSO GmbH

Sandra Hedtke

Novartis

Dr. Christian Matz

Roche

Alexandra Gonzalez

Boehringer Ingelheim

John Carey

Ardmac Group

Cornelia Haas

VTU Engineering

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