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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...

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Article

July 6, 2026

Roller Compaction in Modern Oral Solid Dose Development. Roller compaction has become an increasingly important technology in OSD development ...

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expertXchange

June 10, 2026

Expert Insights: Brian Blagg

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Article

June 8, 2026

Beyond “Brick Dust”: Enabling Technologies for Oral Targeted Protein Degraders

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Article

May 27, 2026

Early Decisions, Faster Launch: Optimizing combination Product Commercialization

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Article

May 21, 2026

Advancing Sterile Liquid Development: Enabling Integrated Solutions for Small Molecules and Biologics

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Video

July 8, 2026

Accelerating Drug-Device Combination Product Development from Clinical to Commercial

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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

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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.

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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.

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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.

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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.

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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.

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Whitepaper

October 13, 2023

The Challenge of Pharma Package Design for Manufacturability

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Whitepaper

October 11, 2023

The Challenges of Scalability in High Potent Manufacturing

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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.

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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

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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.

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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.

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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.

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