Newsletter | January 30, 2023

01.30.23 -- Defining The RNA Therapeutics Industry In 2023

 
Featured Editorial
Industry Insights
How Your Stainless-Steel Column Is Like A French Press

Understanding how purification columns work can help operators better conceptualize the process, enabling greater process understanding and troubleshooting.

Monoclonal Antibody Development For Commercial Success

With roughly 90% of all drugs failing to make it through clinical trials, accelerating the first step of getting to the clinic with a new mAb candidate is crucial.

Elemental Impurities Risk Assessment For Finished Drug Products

This webinar reviews the impact of regulatory changes related to elemental impurities testing, guidance on the best routes to compliance, and an overview of the elemental impurities risk assessment process.

AAV Manufacturing: From Concept To Ready-To-Use Platform

Review the critical parameters for scalable production during upstream and downstream process development, with details on achieving scalable transfection in adherent and suspension platforms.

Longhorn’s Path To A Universal Influenza Vaccine

Thanks to the long-term planning of one biopharma family and some help from the U.S. Army, a universal influenza vaccine is coming soon to a clinical trial near you.

How Membrane Prefilters Enhance Bioprocessing Efficiency

Explore studies that highlight the benefits of prefiltration for increasing the throughput capacity of sterilizing-grade filters challenged with streams containing a wide range of particle size distributions.

CDMO Expertise Accelerates Biologics Development, Manufacturing

An experienced contract manufacturer can help drug developers to better utilize internal resources, leverage deep industry experience, and mitigate risk across development cycles.

Cleaning Validation And Verification In A Highly Potent Granulation Suite

Taking an effective approach to cleaning equipment is paramount. Process experts share more about cleaning validation and verification, the differences between the two, and why they’re so important.

Confident O-Glycosylation Site Identification For ENBREL (etanercept)

Explore the utility of electron capture dissociation (ECD) on the SELECT SERIES Cyclic IMS instrument for unambiguous assignment of glycosylation site locations for 11 Oglycopeptide species of ENBREL.

Is Your Sterile Injectable Ready For Changes In Raw Materials?

Changes in raw materials are inevitable over a drug's lifespan, but even small modifications can throw your drug out of compliance. Learn how to safeguard drug integrity when raw materials change.

Tackling Supply Chain Challenges With Multisite Manufacturing
Gain a more thorough understanding of single-use technology, security of supply, and business continuity management, as well as the need to take action to benefit from multisite manufacturing.
Understanding The Cold Durability Performance Of Fluoropolymer Bags

Although polymer bags are an excellent choice for cold chain use, not all polymer films perform the same way, even if their specifications rate them for use at low temperatures.

Solutions
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