01.19.24 -- WHO Guidance Seeks To Reduce Antimicrobials In Pharmaceutical Liquid Waste

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.

Learn how to interpret the Annex 1 container closure requirements, develop deterministic analytical methods for CCIT, and design packaging studies that generate robust data demonstrating good CCI.

Automated manufacturing is a powerful but often misunderstood tool available to produce drug delivery and other pharmaceutical devices — whether established designs or innovative new ideas.

In Best Practices for Outsourcing Process Development, a panel of experts discussed four themes that may help drive the best outcomes when vetting process development service providers.

Aseptic blow/fill/seal systems for packaging pharmaceutical liquids incorporate materials and processes that provide critical advantages for sustainable initiatives.

Overcome the challenges associated with the lyophilization of biologic drug products by streamlining the scale-up of lyophilization from development to commercialization with the use of scalable technologies.

In the fast-paced and highly regulated world of biotech and pharma manufacturing and operations, achieving operational excellence is paramount, and a skilled program manager is an invaluable asset.

Performing stability studies is a critical step in the drug development process. Discover the ways to ensure that your drug is safe and effective as it goes to market.

Aside from the level of shear or ‘gentleness,’ a number of other factors help determine which type of blender will work best in certain applications. Explore considerations for blender selections.