Newsletter | July 31, 2024

07.31.24 -- An Updated Perspective On The Federal Segment

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Bioprocess Online is excited to introduce Bio-Expo Live, a series of live virtual events designed to empower biopharma professionals with the chance to conveniently explore the newest equipment and offerings in Upstream Bioprocessing, Downstream Bioprocessing and Bioprocess Quality, Data, and Analytical Solutions. Registration is free, reserve your spot today!

FEATURED ARTICLE

An Updated View Of The Federal Segment: VA Formulary Management

As the largest integrated healthcare provider in the U.S., Veterans Affairs presents tremendous opportunity for life sciences companies. This article provides actionable information about the VA's drug benefit design, drug pricing, clinical guidance, and formulary placement and management.

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PDA/FDA Joint Regulatory Conference 2024

The PDA/FDA Joint Regulatory Conference 2024, the only FDA co-sponsored pharmaceutical CGMP conference, is taking place 9 to 11 September in Washington, D.C. Now in its 33rd year, the conference will offer a comprehensive agenda with substantive technical sessions and practical case studies that provide insight into the effective application of Current Good Manufacturing Practice (CGMP).

INDUSTRY INSIGHTS

Site Optimism Sparked By Feedback: A Conversation With Ken Getz

Immerse yourself in this conversation between Greenphire CEO Jim Murphy and Ken Getz, a distinguished figure within the industry, regarding industry trends and providing site support.

Innovative Softgel Technologies To Deliver Poorly Soluble Molecules

Learn how to expedite the development pathway for early phase compounds and how lipid based formulations provide an innovative approach to enhance bioavailability for challenging molecules.

Take A Next-Gen Conjugate Through Lead Candidate Selection, Development

Optimizing and scaling up ADCs can be a significant hurdle. Gain the knowledge and practical guidance needed to navigate the design, development, and manufacturing of next-generation bioconjugates.

Using Advanced Mass Spectrometry To Analyze APIs And Impurities

Characterizing impurities through advanced analytics is a critical step in ensuring biotherapeutic product quality. Learn more about the growing role of CDMOs in developing these products.

How Better CRO Project Management Tools Can Pay Off

CROs are being challenged by siloed project management. Uncover how these obstacles can be overcome with the right technology and approaches for more positive trial outcomes.

Completed Clinical Trials, Terminations Both Rose In 2023

Widespread growth in completed trials is coupled with higher success rates across multiple therapeutic areas, signaling the end of pandemic-related disruptions and infectious disease-related activity.