Evolution in Aseptic Processing: Flexible and Reliable Solutions
The 2020 ISPE Aseptic Conference will focus on providing flexible and reliable solutions for the implementation and management of the latest in aseptic, barrier, containment, and aseptic best practice technologies, including Automated Visual Inspections. Now in its 29th year, this year’s program will feature regulatory and industry experts from FDA, SKAN, F. Hoffman La Roche, Bosch, Fresenius Kabi, Evonik, Merck, and many others to provide your company with the practical tools to improve your manufacturing capability and reliability. Case Studies representing innovative large and small-scale facility and process design will offer insights into successful projects designed to meet unique customer and patient needs.
Now in its 29th
year, this signature event has established itself as the pharmaceutical
industry's leading source on advancing aseptic and barrier operations and
providing invaluable opportunities for peer-to-peer learning through
interactions with industry and regulatory leaders—making the presence of the Boston
Area Chapter important.
the course of two days, you will:
Explore the hottest topics in aseptic
manufacturing, like robotics, ATMPs, and cell therapy scale-out planning
Join industry-critical conversations during an
interactive panel discussion on automated visual inspections and the event
favorite—the interactive regulatory panel
Make valuable connections at the largest
aseptic networking event with 400+ professionals during multiple networking
opportunities, such as small group breakout hot-topic discussions
Plus, maximize your experience with in-depth
training covering four essential areas of
pharmaceutical manufacturing on 4–5 March
Friedman, Deputy Director, Science and Regulatory
Sausville, Director, Div. Case Management, FDA/CBER
David Doleski, Compliance Head for Biologics Quality Operations, Sanofi
Riedel, CEO, Claranor SA
Eugen Goidenko, Executive Vice President, Bausch Advanced Technologies Inc.
Dawn Watson, Director, Microbial Control & Sterile Site Support Sterile &
Validation COE, Merck & Co., Inc.
Who Should Attend?
Sterile Products Processing Community of Practice
Engineering system owners or project managers responsible for aseptic processing equipment
Validation personnel responsible for aseptic processing equipment qualification
Quality Assurance personnel responsible for maintaining the integrity of aseptic systems
Quality Assurance personnel responsible for cleaning and prevention of cross contamination
Equipment manufacturers and suppliers providing state-of-the-art aseptic technology including robotics
Aseptic manufacturing professionals and management
Aseptic processing consultants and regulatory specialists
Manufacturers of design, facilities, building, commissioning, validation
Quality Systems/Assurance and Quality Control (QA/QC) including microbiology professionals
Compounding pharmacy and small-scale facilities professionals
Industrial Hygienist for operational safety in aseptic processing
Professionals new to Aseptic processing and product protection