Manufacturing

Jennifer Markarian is a contributing editor for 

Articles

Experts at Hovione describe progress being made in understanding how to optimize continuous processes for oral solid-dosage drug products. 

Gaining Experience in Continuous Manufacturing

Cynthia A. Challener is a contributing editor to Pharmaceutical Technology.

Understanding and overcoming excipient variation are crucial for successful continuous processes.

Key Ingredients Needed to Drive the Success of Continuous Manufacturing 

Michael Thompson is a professor at McMaster University.

Kevin O’Donnell is R&D manager at DuPont Nutrition & Biosciences

Using a specific addition method to wet the powder bed in twin-screw granulation using a foam binder improves robustness for continuous solid-dosage drug product manufacturing.

Innovating Continuous Twin-Screw Granulation with Foam Delivery

Real-time monitoring and the principles of quality by design were used to optimize an OSD coating process.

Using Industry 4.0 to Optimize Oral Solid Dosage Form Manufacturing

The continuous manufacturing platform can be used for individual unit operations or a complete solid-dosage manufacturing line and can be integrated with third-party equipment.

GEA Aims to Expand Access to Continuous Manufacturing with ConsiGma 4.0

Lisa Graham leads the analytics engineering team at Seeq Corporation. She holds a Ph.D. in chemical engineering and is a registered professional chemical engineer. With 20 years of experience across many industries, her technical strengths include chemical engineering, product development and process model development. She has a well-developed acumen in crafting process analytical technology and data analytics solutions to help drive innovation and growth while reducing costs.

Advanced analytics streamlines continuous manufacturing by providing improved insights to data.


Advanced Analytics Delivers Continuous Manufacturing Innovation

Jennifer Markarian is manufacturing reporter for Pharmaceutical Technology.

Tools help improve understanding of excipient risk in formulating OSD drugs.

Mitigating Risk in Formulating with Excipients

Agnes Shanley is senior editor of Pharmaceutical Technology.

Long a staple for quality by design and solid dosage form manufacturing, design of experiments is becoming an integral part of biopharma upstream process development.

Design of Experiments Gains Ground in Biopharma Development

Systems-based pharmaceutics case studies, challenges, and new uses were discussed at PSE’s Advanced Process Modeling Forum.

Process Modeling Tools Find Use in Bio/Pharma R&D and Manufacturing

CPI, the University of Strathclyde, GSK, and AstraZeneca Collaborate on a continuous direct compression digital twin for pharmaceutical formulation optimization. 

Manufacturing, Continuous Solid Dosage Processing