We are excited to join ASEPTCONN AG at the 3rd Aseptic Biopharma Processing Summit, happening October 29-30. Join us to explore the latest advancements in aseptic processing!
About the Event
As revised Annex 1 regulations come into force, what impact will they have on the pharmaceutical industry? How are manufacturers raising the bar in product quality? What updates should be noted regarding Contamination Control Strategy? The 3rd Aseptic Biopharma Processing Summit will explore the latest in aseptic processing advancements, quality risk management, robotics and automation, microbial monitoring, automated inspection, and more. This conference will be a key gathering for insights into parenteral production, GMP standards, cutting-edge facility design, machine engineering, and quality assurance practices essential for audit readiness.
Over two days, experts will share their knowledge on fill-finish tech transfer, aseptic process simulation (APS) validation, barrier technology, lyophilization, innovative models in aseptic manufacturing, and advancements in sealing and packaging technology, including PUPSIT. Participants will be immersed in the newest regulatory updates, progress in cleanroom technology, and strategies for contamination control, with a focus on enhancing workforce skills for aseptic environments. Additionally, sessions will highlight the role of virtual reality in training and sterility assurance, offering attendees practical insights and tools for improving their manufacturing processes and ensuring compliance with regulatory standards.
Join us at the 3rd Aseptic Biopharma Processing Summit in Vienna, Austria, on October 29-30. Connect with professionals from pharma production, engineering, quality control, quality assurance, regulatory sectors, and technology providers to gain diverse insights, exchange knowledge, and drive innovation in the industry.