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.

TESTIMONIALS