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Webinar: Continuous manufacturing: excipient characterization and formulation development
Continuous manufacturing: Excipient characterization and formulation development
Join our inspiring webinar on continuous manufacturing, with two experts in the field.
Each presentation will last 15 minutes, followed by a dedicated Q&A session, giving participants the opportunity to engage with the speakers and discuss their latest research.
Presentation1:
Development and Implementation of a Continuous Manufacturing Process for a Complex Modified Release Formulation
Key Learnings:
- In less than six months, a modified-release formulation and process were developed for clinical supply using continuous direct compression.
- NIR and RTD models were developed as part of the control strategy to ensure content uniformity of both the API and the release-controlling polymer.
- A dissolution model was calibrated in the laboratory and successfully implemented at scale to monitor dissolution in real time.
Presentation 2:
Rheological powder characterization of excipients to understand their behaving during feeding
Key Learnings:
- Understand how powder flowability can be characterized by rheological analysis
- Translate the results into predicting powder flowability into feeders within a case study
Date & Time & Timezone: Mar 12, 2026 05:00 PM CET Amsterdam, Berlin, Rome, Stockholm, Vienna
For more information & registration here:
Speaker:
Dr. Vanessa Havenith
Technical Sales Manager, SE Tylose GmbH & Co. KG
Dr. Vanessa Havenith studied and obtained her doctorate in mineralogy at RWTH Aachen University. After completing her studies, she worked as Technical Sales Manager for SE Tylose GmbH & Co. KG in the field of industrial applications (building materials, petroleum and paints) from 2012 to 2021. In 2021, she moved to the pharmaceutical sector, where she is responsible for various key accounts within Europe as Technical Sales Manager.
Ricardo Sousa
Senior formulation development scientist, Hovione
Ricardo Sousa has a background in Biological Engineering and over 12 years of experience in pharmaceutical development, which contributes to a solid understanding of pharmaceutical sciences and technologies.
Throughout his career, he has developed technical expertise across spray drying, batch and continuous tableting, dry and wet granulation, and process analytical technologies. He is also skilled in modelling, data analysis, and statistical methods, supporting robust process understanding and optimization. In recent years, Ricardo has been mostly involved in continuous tableting, serving as the lead scientist for several projects conducted on the CDC‑10 line in Portugal
For more information & registration here:
Source: Dr. Vanessa Havenith, Ricardo Sousa, Pharma Excipients, webinar Continuous manufacturing: excipient characterization and formulation development
