12.06.24 -- The 4 Technologies Poised To Transform The Pharmaceutical Supply Chain In 2025 And Beyond

The pressure-sensitive bisect design allows accurate tablet splitting by maximizing facet width, optimizing angles, and balancing radius values for durability and user-friendly administration.

To keep up with oligonucleotide demand, manufacturing needs to shift toward larger-scale processes, but this scale-up process brings challenges that must be addressed.

Learn how specialty pharmaceutical company Noven Pharmaceuticals successfully launched a new computer system validation by upgrading their enterprise resource planning system.

Investigate the advantages and disadvantages of single-use technologies and stainless steel systems with a focus on performance, adaptability, and economics.

Gain insights that can support your next steps, whether advancing to a new clinical phase, constructing a new facility, or fine-tuning an existing process to keep pace with market shifts.

Rethinking your company’s SOPs to reduce carbon emissions and ensure more sustainable workflows is no easy feat. The key is looking at these initiatives as a crucial, community-driven effort.

Analyze and review different containment methods and help determine which would be most beneficial for your first (or next) containment device to ensure personnel protection.

Technological developments have led to growth in the suitability of fermentation. Explore the impact of the evolution of synthetic biology and supporting technologies on modern fermentation practice.

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

Discover how a non-destructive method can be developed to test container closure integrity in autoinjectors equipped with an optically transparent window.

In the event of an IV bag leak, contaminants can adversely affect the solutions within. See how the reference standard for CCIT, USP 1207, applies to the CCIT inspection method of IV bags.

Learn why proper training is vital in cleanroom cleaning and disinfection and how to develop and maintain a successful training initiative.

Review advanced retrosynthetic analysis services and how these tools empower better, more efficient development of innovative small molecule drugs.

Gain insight into the limitations of conventional research models, how Organ-Chips are helping researchers bridge the translation gap and overcome pervasive barriers in drug development, and more.

Risk assessment is integral to manufacturing processes, particularly in drug production, and having effective containment strategies can help identify potential hazards and ensure worker safety.

Discover key strategies for seamless pharmaceutical technology transfers that accelerate time to market, ensure product quality, and meet regulatory standards across the drug lifecycle.

Explore how a solvent-free alternative for the production of amorphous solid dispersions (ASDs) not only improves manufacturability but also reduces the carbon footprint of ASD manufacturing.

A leading CDMO raises the bar in the delivery of pharmaceutical ingredients with its fit-for-purpose small molecule development and manufacturing capabilities and its new approach to project management.

Learn more about a differential scanning calorimeter that offers thermal stability screening of buffer formulations and protein sequence modifications.