Newsletter | March 7, 2023

03.07.23 -- How Collaborative Value Engineering And Continuous Improvement Enhance The CDMO Relationship

Industry Insights
How Collaborative Value Engineering And Continuous Improvement Enhance The CDMO Relationship

Regular assessments of a partnership’s value in terms of supply chain, operational efficiency, data analysis, and more can optimize and extend the product life cycle.

Match Your Development And Manufacturing Path To Your IND Milestones

The drug development journey is long, expensive, resource straining, and risky. Discover how to maximize the value of early-phase material and match your development path to your IND milestones.

Use Of Filtration Plates For Purification Of DNA Samples For Sequencing Library Preparation

Discover how we examined a DNA sample purification method employing 96-well filter plates as an alternate to organic extraction.

Process Effects On Drug Product Quality In Pharmaceutical Manufacturing: A Validated Measurement Process

This white paper discusses the importance of understanding how critical process parameters can impact a product’s critical quality attributes, and how a systematic approach with validated SPR assays can help in this respect.

Speed-To-Market: API Large-Scale Commercial Manufacturing

A pharmaceutical company was looking to partner with a CMO with commercial manufacturing capabilities, large-scale assets, multinational sites, and exemplary quality systems/U.S. FDA track records.

Early Development To Clinic: De-Risking A Bioconjugate’s Journey

The journey of a novel bioconjugate into the clinic is complex and uncertain. Explore the particular challenges when moving a bioconjugate candidate from early development into the clinic.

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