expertXchange October 13, 2026 The Critical Role of Fill-Finish in Large-Molecule Manufacturing. Explore how temperature management, pump selection, isolator technology, and inspection help preserve sensitive biologics during sterile manufacturing. More
expertXchange September 28, 2026 From vials to pre-filled syringes: development considerations for a successful transition. Key considerations for formulation, container compatibility, sterile fill-finish and device performance when moving an injectable drug product from vial to PFS. More
expertXchange July 27, 2026 Supply Chain Fragility in Sterile Injectables: Supplier dependencies, outsourced sterilization, and transportation conditions can introduce sterility risks that extend far beyond the cleanroom. More
expertXchange February 18, 2026 5 Critical Pre-Use Post-Sterilization Integrity Testing (PUPSIT) Considerations For Sponsors Targeting The EU Market. PUPSIT is the process of performing filter integrity testing on sterilizing filters More
expertXchange February 9, 2026 Expert Insight: Positioning Australia as a Global Gateway for Clinical Trials. Insights from Michele Stokes, VP APAC & GM, PCI Melbourne More
expertXchange February 6, 2026 Targeted Modalities Set Elevated Standards for Precision. A look at the development and manufacturing processes needed to produce them. More
expertXchange December 8, 2025 From Clinical to Commercial: Introducing Devices Earlier to Streamline the Drug-Device Combination Journey. Achieving scalability, flexibility, and integration from Phase I to Commercial Launch More
