10.01.24 -- Team Topologies For Outsourced CMC Development

Examine the critical role of inspection systems, specifically metal detectors, X-ray systems, and checkweighers, in pharmaceutical manufacturing.

Business leaders can enhance QC operations by adopting a holistic view of the quality ecosystem and embracing comprehensive modernization strategies. Explore four principles for greater QC lab agility.

Learn about the advantages and disadvantages of CCI testing methods, how the revised EU Annex 1 may impact your strategy for ensuring CCI of sterile pharmaceutical products, and more.

Whether bringing a novel therapy to market or altering current devices, companies must determine the best selection for administration without impacting drug efficacy, quality, and safety.

Formulators have many choices when it comes to bioavailability enhancement. Which should you use for a given compound? Explore tools to predict the performance of bioavailability-enhanced formulations.

Watch to hear Steven Facer, Adare's Vice President of Business Development EU/ROW, discuss the challenges of pediatric oral solid dose manufacturing and how to overcome them.

A commercial packaging solution can be the first and enduring impression that a sponsor company makes on a patient, and its suitability can impact a biologic’s commercial success.

See how a platform that leverages polymeric implantable drug delivery systems enables improved bioavailability, patient compliance, and mitigation of issues associated with repeated injections.

Discover how this single-use bioreactor system optimizes cell growth and simplifies tech transfer.