In these short blog posts, our experts delve into the intricate world of formulation, development, and manufacturing of OSD and DPI products and clinical trial supply services for a range of finished dose modalities, packaging configurations, and temperature requirements.
Join us as we explore the latest advancements, insights, and challenges shaping vital areas of pharmaceutical innovation.
For small pharmaceutical companies navigating the intricate path from discovery to commercialization, the choice of a Contract Manufacturing Development Organization (CDMO) partner for your Chemistry, Manufacturing and Control (CMC) needs is one of the most critical decisions. The right partner does more than ensure compliance—they become a strategic ally in […]
Read MoreDive into the journey of turning a powder formulation into a finished pharmaceutical product. This blog explores the hurdles in achieving optimal product yields when filling capsules for dry powder inhalers (DPIs). The Impact of Powder Fillability Imagine that a pharmaceutical development team has discovered a promising new formulation intended […]
Read MoreFor any clinical trial, a reliable supply chain for investigational products and materials is essential to ensure that trials run smoothly, meet regulatory standards, and maintain the integrity of the data. To successfully achieve this, many clinical trial sponsors decide to partner with a specialized clinical trial supply service provider. […]
Read MoreWhat is Spray Drying? Spray drying has become an invaluable technique in the pharmaceutical world, particularly for transforming liquid formulations into dry powder, a critical step in developing inhalable therapeutics. Fast and cost-effective, spray drying allows precise control over particle characteristics such as size, stability, and solubility, making it ideal […]
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