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The Hidden Complexity of Capsule Development
March 24, 2026
As small molecule pipelines continue to shift toward more complex, potent and sensitive APIs and as clinical trials similarly evolve toward greater complexity, the linear model of development is no longer sufficiently robust. Instead, success depends... read more
Considerations When Qualifying a Supplier
November 11, 2025
Ensuring the quality of finished products not only requires in-house quality control processes but also a robust supplier qualification process. Establishing a supplier qualification program is one of the most critical quality system activities for a... read more
How CDMOs are Creating Strategic Advantages with Emerging Technologies
March 25, 2025
Modern outsourcing relationships have become more strategic and technologically sophisticated. As these CDMOs and CRDMOs work to stay competitive, they are looking to build capability and expertise in continuous manufacturing, automation, AI-driven ... read more
Closing the Knowledge Gap in High-Potency Drug Development
February 13, 2025
As the industry trends toward more customized, higher-leverage formulations, the development and manufacture of drug products containing highly potent active pharmaceutical ingredients is experiencing a promising growth curve. read more
2025 Predictions: Industry Leaders Weigh in on the Future of Oral Solid Dose
February 06, 2025
New year, new advancements for the industry’s oldest and most beloved dosage form? It’s likely, according to experts. Here’s a look at what industry leaders in pharmaceuticals and nutraceuticals are predicting for the coming year. read more
Meeting Growing API and CDMO Production Demands with Dust Collection Systems
October 01, 2024
As global production of APIs expands, the significance of well-designed dust collection/containment systems has never been more critical in protecting OSD manufacturing. This article offers recommendations and tips for selecting dust collection ... read more
To Facilitate API Quality Agreement Discussions, Let’s Try APIC’s Template
April 01, 2024
Pharmaceutical manufacturing, complex and regulated, operates under stringent requirements, imposing strict standards at every stage of the process from raw materials for the drug substance manufacturing to the drug product distribution. These ... read more
Formulation Development Outsourcing Market: A Comprehensive Overview
April 01, 2024
The pharmaceutical industry is facing a paradigm shift as it moves toward a more streamlined, cost-effective, and time-sensitive approach to drug development. With the growth of formulation development outsourcing, companies are finding innovative ... read more