| New This Week on Bioprocess Development Forum |
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- Step Up to GMP Manufacturing or Outsource to a CDMO: Considerations and Tips
The decision to tackle GMP manufacturing in-house or work with a contract development and manufacturing organization (CDMO) represents a pivotal crossroads in a product’s journey to market.
(Read Article)
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Smarter Downstream Process Development with Modern Tools
Join this event series featuring industry experts in an engaging discussion with peer-to-peer insights. Topics discussed are high-throughput process development, quality-by-design approaches, and an introduction to mechanistic modeling with GoSilico.
(Read Article)
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- Cytiva Upgrades Massachusetts Contract Biomanufacturing Site with Increased Capacity and Automation Technologies
Biotechnology companies looking for assistance in bringing therapeutics to market faster can leverage the extensive technical support and single-use biomanufacturing expertise.
(Read Article)
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- Good Manufacturing Practices: Challenges with Compliance
The complexity of biologics and the use of new technologies present challenges for complying with CGMPs.
(Read Article)
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| Bioprocess Development Forum Topic Spotlight |
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Questions for 2020
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