01.16.25 -- STREAM Edition: Pharmaceutical Manufacturing Insights: From Development To Delivery

Succeed in combination product development by understanding the risk factors that may arise and implementing mitigation strategies that will streamline the device development process.

Discover how Parvulet's unique formulation simplifies medication administration for patients of all ages, especially those with swallowing difficulties.

See how Stevanato Group evaluates each product and its properties and recommends a technology that best suits your requirements.

Gain insight into the risk to container closure integrity (CCI) during deep cold storage and identify appropriate analytical tools, to generate robust data to characterize and mitigate the risk to CCI.

Learn about the fundamentals of UPLC columns, their diverse chemistries, and their versatility in separating small-molecule analytes using reversed-phase and hydrophilic interaction techniques.

Continuous processing in biopharma holds promise in improving efficiency, quality, and scalability. Watch to explore the fundamental principles and operational methodologies of continuous processing.

Examine study findings aiming to assist process development scientists and engineers in understanding the structure of depth filter capsules, identifying key parameters for development, and more.

Learn how you can obtain comprehensive solutions for cleanroom projects that help you ensure regulatory compliance and operational efficiency.

Discover the importance of compressed gas monitoring in ensuring product quality and compliance with EU GMP standards.

Cryopreservation is essential for storing stem and T cells for therapy but poses challenges like low survival and function loss. Watch to explore optimization strategies and solutions.