Continuous manufacturing (flow chemistry) is a key element in the green-chemistry landscape of a pharmaceutical company. In this webinar, Benjamin Martin, PhD from Novartis will use case studies to illustrate the drivers for continuous processing for clinical supplies, the challenges navigated during process R & D, and a summary of how the sustainability metrics, Process-Mass-Intensity (PMI) and Total CO2-Release (TCR), are positively affected.
Hongwei Yang, PhD from WuXi STA will show how industry collaboration between Pharma companies and CDMOs with strong capability to quickly develop or transfer in a flow process and assemble customized lines at plant-scale can accelerate the implementation of continuous manufacturing for drug substance supply with a cost-effective and greener process.
Key Learning Objectives:
- Sustainability metrics for continuous manufacturing (CM) in pharmaceutical industry
- Key drivers for using CM at the clinical stages
- How Innovators and CDMOs can work together to speed implementation of CM and bring therapies to patients faster.
Who Should Attend:
- Pharmaceutical & Fine Chemists
- Academic Chemistry Researchers
- Process & Development Chemists
- Drug Discovery Chemists
Brought to you by:
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Benjamin Martin, Ph.D.
Associate Director Science & Technology Continuous Manufacturing-Upstream Network Leader,
Novartis
![%7B4b7404f2-c109-4686-bd4d-618b18a6dbfe%7D_2022-4-5-Hongwei-Yang-speaker %7B4b7404f2-c109-4686-bd4d-618b18a6dbfe%7D_2022-4-5-Hongwei-Yang-speaker](https://communities.acs.org/t5/image/serverpage/image-id/5874iB521760C334B1232/image-size/large?v=v2&px=999)
Hongwei Yang, Ph.D.
Executive Director and Head of Flow Chemistry,
WuXi STA, a subsidiary of WuXi AppTec
Melissa O'Meara
Forensic Science Consultant,
C&EN Media Group