05.27.25 -- Pharma 4.0 Adoption Needs Cooperation — Here's How To Build It

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.

Understanding top safety concerns, from combustible material handling and chemical exposure to HPAPIs, is the first step toward preventing accidents in biopharmaceutical manufacturing environments.

A design of experiments (DoE) study examined the anion-exchange process in general and to draw possible correlations between such properties and overall viral clearance capability.

Which production model is best suited for your cell and gene therapies, Point-of-Care (PoC) or Decentralized Manufacturing? Uncover the impact of both approaches.

Maintaining drug product sterility and compliance demands rigorous Container Closure Integrity (CCI) within contract manufacturing. Learn how to fortify your processes.

Examine disinfectant residue characteristics, impacts, and removal challenges in cleanrooms, as well as practical requirements for maintaining cleanliness standards and addressing these residues effectively.

A new category of software solutions is emerging that may be the key to digital transformation for life sciences companies. Gain in-depth knowledge about DataOps for manufacturing environments.

Discover advanced approaches to designing robust amorphous formulations and optimizing spray drying processes tailored specifically to difficult-to-formulate compounds.

What is actually behind the procurement of a pharmaceutical labeling machine and how does the process work? You can find out here what the path to your pharmaceutical labeling machine looks like.

See how formulating an orally disintegrating tablet (ODT) created a convenient dosage form with a shorter T_max for the treatment of acute migraines.

Listen to expert insights on selecting the right CDMO partner for large-scale API production as well as key considerations to ensure your small molecule API program is successful.

Explore how you can obtain comprehensive solutions for cleanroom projects that help you ensure regulatory compliance and operational efficiency.