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* Differentiate the suitability, quality and processability of an excipient. * Recognize the significant impact of superior excipient processability. * Understand the economic return associated with excipient selection.
Rethinking Inhalation Drug Development
CDMO Solutions – Reducing Risk and Accelerating Time to Market
Unparalleled Expertise and Transparency Drive a Unique Development, Manufacturing, and Clinical Supply Experience
Streamlined Product Development Leveraging Pharmaceutical Classification Models
Selecting container closure components with confidence: A data-driven approach to container closure integrity
Drug products in development require compatible packaging to meet milestones and gain approval. West supports pharmaceutical partners with a data-driven process to give you confidence with closure containment that meets requirements in the modern regulatory landscape.
Nasal Delivery of Spray Dried Biologics: Opportunities & Challenges