Process Chemistry and Pharmaceutical Manufacturing

Process chemistry is essential for scaling up drug substances from laboratory synthesis to commercial manufacturing. This session focuses on the development of robust, efficient, and cost-effective synthetic routes for active pharmaceutical ingredients (APIs). Topics include process optimization, impurity control, reaction scale-up, crystallization techniques, polymorphism, and process analytical technology (PAT). The session also covers continuous manufacturing, technology transfer, and compliance with GMP standards. Discussions highlight strategies to improve yield, reduce waste, ensure product consistency, and meet global regulatory expectations in pharmaceutical manufacturing.

 

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