Content focuses on the interactions of multidisciplinary functions and discusses the scientific application of experimental design methodologies as part of the product manufacturing process. Individual topics could include formulation, clinical phases, manufacturing, technology transfer, production scale-up, and optimization.
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ISPE in the News
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ISPE Training: Process Validation Training Course, 8 - 10 April
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Discover Exciting Career Opportunities on ISPE's Job Board
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Steele Appointed Acting Director of US FDA's CBER
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US FDA to Cut Back on Routine Inspections
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Tariff Threats Create Uncertainty in Pharma Market
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Expecting the Unexpected Ensures Continuity in Biopharma Manufacturing
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Digital Twin may Streamline Gene Therapy Production
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AMT Designation Granted to Cellares' Cell Shuttle
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Innovative Culture Media Support Intensified Processes
- Navigating Category 3 Compounding Challenges
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May / June 2024
The commercialization of personalized medicine has ushered in demand for a new type of facility—…
November / December 2023
There is much that large-scale commercial stem cell therapy processes can adopt from the existing…
May / June 2022
Realizing the promise of any novel viral vector therapeutic depends on the innovator’s ability to…
Lifecycle Approach to Biotech Process Validation
This discussion paper proposes ideas for answering the questions about the application of the…
Stage 3 Process Validation: Applying Continued Process Verification Expectations
This discussion paper proposes ideas for answering the questions “How is Stage 3 monitoring and…
