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About the webinar

Crystallization remains one of the most complex and impactful stages in pharmaceutical process development, determining critical attributes such as purity, particle size distribution, and downstream processability.

If you want to learn more about strategies for achieving robust and controlled crystallization, do not miss this webinar. Case studies discussion will highlight the integration of solubility modeling, and process monitoring to optimize particle properties, yield, cycle time and product quality. Advanced methodologies, including spherical agglomeration, are explored as innovative approaches to enhance particle properties, improve filtration performance and formulation. Emphasis is placed on data-driven decision-making and risk mitigation to ensure scalability and reproducibility in industrial conditions.

Featured speakers in this webinar

Ana Cruz, Ph.D. Senior Scientist at Hovione Ana joined Hovione’s Process Chemistry Development team in 2009 to work on the development of chemical processes for manufacturing Active Pharmaceutical Ingredients (APIs). Graduated in Applied Chemistry from the Faculty of Science and Technology of Lisbon (FCT-UNL) in 2004, followed by a PhD in Organic Chemistry at the University of Bath with Professor Michael Willis.

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