02.14.25 -- Digital Certificates Of Analysis: A Vision For The Transfer Of Quality Data

It is important to develop robust, reliable processes to safeguard APIs. Explore the best practices to provide patients with the highest quality treatment that meets their therapeutic requirements.

Discover the benefits of controlled release, PBPK modeling in controlled release formulation development, and how modified release products can be developed to deliver optimal patient outcomes.

High voltage leak detection (HVLD) and vacuum decay are two of the more common methods used to test container closure integrity. Find out which method is superior.

Setting the lower punch ejection height in your tablet press is crucial to reaching maximum press speed and increasing product yield. Learn how to avoid poorly positioning your punch.

If you’re launching an international clinical trial, consider the noteworthy benefits of partnering with an in-country depot, including increased efficiency, reduced costs, and reliable access to raw materials.

Uncover more on cleanliness detection, contact-angle measuring methods, the water drop surface energy test, and in-situ particle monitoring.

As capabilities and resources grow throughout a project, both become strained in-house and the scale-up process becomes a steeper hill to climb. Reveal why potential CMO partners should be able to help. 

Srinivasan Shanmugam, Ph.D., Executive Director of Pharmaceutical Sciences at Adare, discusses pediatric patient compliance, regulations impacting trial access, excipients within formulations, and more.

Delve into the significance of adept interpersonal leadership within your drug safety program, shedding light on the operational and financial benefits that stem from fostering a collaborative environment.

The modernization of QC laboratories demands a more holistic approach and necessitates a broader perspective of different systems. Continue reading to discover the best way to achieve these results.

Gain insight into a “simul-spray” process pioneering for combining small and large molecules into a single, atomized drug product for inhalation administration.

Aseptic filling technology is of utmost importance. Explore in great detail an aseptic filling solution that has been specifically designed for laboratory and R&D applications in the pharmaceutical industry.

Unveil how medical device companies aim to balance patient safety with environmental stability by offering bio-based UHMWPE, reducing carbon footprints by up to 70%.