Newsletter | December 20, 2022

12.20.22 -- 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.

Engineering Approaches To Respiratory Drug Delivery: Mannitol Case Study

This article presents a case study that explores the material and performance properties of spray-dried and jet-milled mannitol for respiratory delivery of crystalline mannitol.

Overcome Complex Protein Challenges With Optimized Expression

Realizing the potential of next-generation molecules calls on appropriate expression technologies and development processes that can facilitate their path to market.

Integrated Predictive Sciences Solutions To Accelerate Drug Discovery

Learn how having the right predictive sciences capabilities integrated into R&D workflows delivers a scientific decision support environment that reduces time and expense, improves quality, enhances collaboration, and accelerates innovation in bringing new drugs to market.

Are End-To-End CDMO Partnerships The Solution To Drug Development And Manufacturing Upheaval?

Growing complexity and risks in drug development and supply have implications for outsourcing models. See how to structure and manage CDMO partnerships for a future full of uncertainty and disruption.

A Human HTS Platform For Assessing Gastrointestinal Toxicity (GIT) Risk In Early Development

We review a solution for the need for human models of GI risk assessment that can be utilized for drug optimization in early development.

Purifying Tagged Proteins Using ÄKTA Go Protein Purification System

ÄKTA go is a small and compact liquid chromatography system that allows researchers to perform routine protein purification with ease while allowing for efficient use of bench and cold cabinet space.

Delivering Pre-IND To IND Safety Studies In Just Three Months

A biotech company partnered with an integrated research, development, and manufacturing services company to deliver pre-IND to IND safety studies for a treatment therapy for gut-brain diseases.

Spray Drying For Improved Solubility

In a recent webinar, experts discussed how to develop a spray-dried powder formulation and scale it from early feasibility studies to commercial manufacturing.

Reduce Protein Biologic Development Risk

Explore the process of assay development, qualification, and validation for critical potency assays and how Sartorius supports customers through this vital step.

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