01.12.24 -- To Thrive In A Highly Regulated Manufacturing Environment, Improve Your Flexibility

What makes a next-generation CHO bioproduction process? Take a journey through areas of innovation for creating expression systems of the future, with a focus on DNA and cell expression technologies.

Inspection technologies play a crucial role in ensuring the safety, quality, and reliability of tablet and capsule packaging. Explore package integrity testing methods proven to be accurate and efficient.

Patients are more empowered, making it essential to promote better adherence, improve medical benefits, and bolster market perception. See the technologies enabling this shift toward patient centricity.

This conversation focuses on sustainability in bioprocessing and the exciting advancements happening in the space, featuring practical examples and case studies.

High-concentration formulations often present challenges with regard to viscosity as well as potential changes in the behavior upon stability. Discover solutions to mitigate high viscosity.

Investigations into viable air excursions are difficult to perform using traditional methods. Learn why a real-time viable particle counter is key to providing process improvement.

Here, we delve into the significance of the knowledge transfer stage of the pivotal technology transfer process, its key components, and how it ensures the success of the overall tech transfer process.

De-risking RSM and KSM procurement can be accomplished via several means, but local sourcing of raw materials and in-house production have proven tremendously effective.

We dive into the DSC testing and analysis of pharmaceutical materials to better understand how to obtain accurate results and avoid potential problems with data interpretation.

Explore aqueous detergent selection criteria as it fits into three broad categories: function and efficacy, health and safety, and environmental.

Learn about a platform for creating injectable and implantable long-acting drug delivery products, including the technical basics and how it can be used to deliver small molecules, peptides, and biologics.

In the CCIT space, one single inspection technology cannot be used for every type of pharmaceutical product. You should always weigh the various factors to determine the ideal inspection methodology.