04.04.25 -- The Evolution And Future Prospects Of ASTM International Cleaning Standards

Walk through the rigorous inspection process pharmaceutical products undergo to ensure safety and quality, from granulated ingredients to packaging.

Gain insights from a pharmaceutical equipment manufacturer on factors cannabis manufacturers should consider when they're looking to purchase a mixer.

Explore more about heat tunnel particle monitoring. Join Marc Machauer and Mark Hallworth to discuss basic principles, viable/nonviable monitoring, and probe placement strategies.

Throughout the pandemic, painkiller and sedative demands spiked. Drug manufacturers and CDMOs have become critical in efforts to stabilize the supply of Bupivacaine HCl and other essential drugs.

Sterility assurance requires robust programs from raw materials to facility design. Learn about best practices, misconceptions, and the importance of environmental monitoring and regulatory compliance.

Here, we provide systematic methods to increase return on investment. Discover the seven primary investment recovery channels.

Find out how companies can de-risk their device selection as they bring this new generation of high-volume, high-viscosity biologics to market.

Learn how orally disintegrating tablets act as a patient-centric solution to various factors that impact treatment adherence rates across various diseases.

Complementary analytical techniques like DSC, MDSC, cRHp, DVS, and SolCal accurately quantify amorphous content in pharmaceuticals to ensure stability, compatibility, and efficiency.

Traditional aseptic filling solutions can introduce contamination and variability. See how commitment to finding innovative solutions and improving patient outcomes can enhance processes.

Characterizing Fab and Fc-Fusion proteins and developing robust manufacturing processes can help usher them to market and provide new treatment options for diseases that are challenging to treat.