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BIOPHARM INTERNATIONAL 2011 WEBCAST SERIES
BioPharm International is pleased to present its 2011 Web Seminar Series, addressing key issues in process development and bioprocessing. These one-hour sessions include presentations by industry experts and interactive dialogue with the audience. Watch live and participate in the Q&A, or catch them later on demand. |
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Webcasts: |
Bio-G Webinar - Real-Time Scheduling of Biomanufacturing Supply Chains
Thursday, June 23, 2011. 1:00PM Pacific - Biomanufacturing Supply Chains are unique in their need to account for variability and risk in bulk, fill and packaging production and inventory positioning. We'll describe a different approach to biomanufacturing supply chain planning that optimizes inventory levels and risk strategies in real time. We'll show how by focusing on real-time data from PI, Delta V, Oracle, SAP, Excel and other sources, biomanufacturers can quickly re-plan against real-time events in seconds rather than hours or days.
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Featured Whitepapers: |
Keys to reducing time-to-market
With development times measured in years, increasing costs represent a major challenge confronting pharmaceutical and biotechnology companies. As a result, reducing time-to-market is an essential component in any business strategy.
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Advertiser: Vetter Pharma International GmbH
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Finding the right contract manufacturer
With fewer blockbuster drugs in the pipeline, companies are on the lookout for an enduring solution to meet market challenges. To maintain or expand market shares, pharmaceutical companies must devise new strategies to remain competitive.
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Advertiser: Vetter Pharma International GmbH
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A Conversation with BIO's Jim Greenwood
Jim Greenwood comments on the state of innovation in the bio/pharmaceutical industry and discusses policies that could help move promising technologies out of discovery and into development. Podcast interview by Editor Director Michelle Hoffman.
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Answers to Your Questions about QbD
Hundreds of listeners tuned into our recent web seminar on Quality by Design, and we didn?t have time to answer all their questions. Fortunately, our speakers gathered to answer the common questions in this podcast. Listen to hear their views.
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The Current State of Supply Chain Security: An FDA Perspective
In this interview, Richard L. Friedman, Director of the Division of Manufacturing & Product Quality in the Center for Drug Evaluation and Research, FDA's Office of Compliance discusses the progress made so far in executing supply chain security programs.
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