Critical Quality Attribute Monitoring and Control in Drug Substance Manufacturing II
AIChE Annual Meeting
2016
2016 AIChE Annual Meeting
Process Development Division
Oral
Continental 4
Hilton San Francisco Union Square
Wednesday, November 16, 2016 - 3:15pm to 5:45pm
Developing robust drug substance production processes to ensure patient safety and drug efficacy is dependent on the sound understanding and control of the drug substance quality attributes relevant for clinical performance and drug product manufacture. This understanding is then translated into the design of the drug substance manufacturing process and a relevant monitoring and control system to ensure that quality attributes within the desired ranges are consistently obtained. This session covers drug substance critical quality attribute identification, characterization, and monitoring systems for both drug substance quality and manufacturing process control. Authors are encouraged to highlight clinically relevant specifications for drug substance and innovative control strategies for drug substance manufacturing.
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Pricing
Individuals
AIChE Pro Members | $150.00 |
AIChE Graduate Student Members | Free |
AIChE Undergraduate Student Members | Free |
AIChE Explorer Members | $225.00 |
Non-Members | $225.00 |