Article September 3, 2026 Roller Compaction: Stable, Continuous OSD Manufacture. A technical overview of how compaction force, roller gap, milling and containment shape robust dry granulation strategies for OSD products. More
Article September 1, 2026 Sponsor-facing platforms: the other side of clinical trial digitalization. See how digital collaboration environments can simplify regulatory, financial and supply chain oversight while supporting informed sponsor decisions. More
Article August 18, 2026 Biologics, GLP-1s driving evolution of fill-finish manufacturing. Growing injectable pipelines are changing how manufacturers approach sterile capacity, automation, isolator technology, and scalable CDMO partnerships. More
Article August 18, 2026 Ahead of the Curve: Strategic Investments for Outsourcing Partners. Explore the investment priorities shaping future CDMO networks, from scalable sterile manufacturing and advanced delivery formats to integrated global capabilities. 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
Article July 13, 2026 Optimizing Impact for Rare Diseases. Rare medical conditions can do more than substantially affect wellbeing. They can also make sufferers feel discouraged or even hopeless about their prospects for successful treatments... More
Video July 8, 2026 Accelerating Drug-Device Combination Product Development from Clinical to Commercial 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
expertXchange December 1, 2025 Common Challenges in Early Clinical Trial Planning. Early clinical trial planning sets the foundation for success when navigating packaging, labeling, and logistics for your first-in-human study. More
expertXchange August 19, 2025 Navigating Global Trade Complexities in Pharma: Tariffs, VAT, and Free Trade Zones Explained. understanding how to manage trade compliance and optimize international supply chains is more critical than ever. More
expertXchange May 12, 2025 Pre-IND and Distribution Strategies: Ensuring Efficient Clinical Studies. Navigating the complexities of early-phase clinical trials requires strategic foresight and regulatory expertise. More
expertXchange March 27, 2025 Unlocking the Benefits of Customs Warehouse for Pharmaceutical Supply Chains. The global pharmaceutical supply chain is becoming increasingly complex, with regulatory requirements, tax implications, and logistical challenges. More
Webinar August 12, 2024 Clinical Trial Directive to Clinical Trial Regulation - Transition. With just over five months left of the legal transition period, it is vital that sponsor companies strategically plan ahead. More
Whitepaper June 15, 2023 Digital Transformation: A Critical Component for CDMOs in the Pharmaceutical Industry. Digitization is now a strategic capability for CDMOs in providing pristine customer service to their clients. More
Whitepaper July 15, 2022 Optimizing Your Clinical Trial to Commercialization Journey. The average cost of a delayed new drug launch is $15 million per day More
Q&A October 21, 2025 The current pharmaceutical contract manufacturing landscape. Tim Roberts, chief commercial officer for PCI Pharma Services, explores the current pharmaceutical contract manufacturing landscape. More
Q&A July 14, 2025 Driving Sterile Innovation at Scale. How the acquisition of Ajinomoto Althea in San Diego, CA significantly augments PCI’s sterile fill-finish offering in North America. More
Q&A June 17, 2025 Driving Precision, Agility & Partnership in Complex Drug Development. With the rise of targeted therapies, complex biologics, and ultra-potent small molecules, the role of pharmaceutical development has evolved. More
