Get the Information You Need to Stay Ahead in this Rapidly Changing Field at ISPE's Biopharmaceutical Manufacturing Conference
ISPE's 2016 Biopharmaceutical Manufacturing Conference will provide you with the knowledge to implement the necessary changes to current facilities or to develop new facilities with sufficient capacity to meet the increasing demand for biologics. We encourage you to bring your entire team – from C-suite to production line. Strengthen your team's ability to operationalize investments and effectively solve issues before they become unmanageable. Comprehensive Track Topics include:
Planning and Managing Capacity Challenge: |
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- Asia Pacific CMO Capacity
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- Large-Scale Demand – Capacity Modeling
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- AE/CM/V Service Provider Capacities
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- Preparing Our Supply Chain for Next- Generation Biologics Manufacturing
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- Raw Material Analytical Methods and Characterization
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Technology Solutions to Meet Capacity Challenge: |
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- Point-of-Care Manufacturing
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- Retrofitting Existing Biologics Facilities with New Technologies
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- Novel Approaches for Purification Strategies
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- Future Development – Technology Platforms
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- Synthetic Biology Approaches/Arteminsinin Production
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- Next-Generation Automation – Bioburden
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- Continuous Processing and Manufacturing – Possibilities, Challenges, and Solutions
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- Next-Generation Equipment and Materials – Bioreactors, SUT, Columns, and Resins: Capacity/Constraints
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- PAT and Controls Strategy
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Accountability for the Human Element: Regulatory, Drug Shortages, and the Patient: |
- Emerging Technologies in Biologics
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- FDA Preparations for Developments in Biopharmaceutical Manufacturing
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- FDA Pre-Approval Inspection Perspective
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Spaces are limited! Take advantage of early bird pricing by registering on or before 4 November 2016. For more information, visit the 2016 Biopharmaceutical Manufacturing conference website.