Newsletter | June 23, 2020

06.23.20 -- High-Loaded Dosage Forms: Novel Platform Expands Dispersion Utility

 
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Telltale Signs You’re With The Wrong CDMO

Is your CDMO an asset or a hindrance? This article explores 10 red flags that signal your parter isn't carrying its weight on your journey to commercialization.

Robust Field Guide To qPCR

qPCR remains the gold standard for validation of microarray and next generation sequencing data and the method of choice for both clinical and basic research labs for a wide range of applications. However, there remains general concern about the production of data that truly reflects the tested experimental conditions. We have developed a comprehensive guide to performing the ultimate qPCR experiment. The following is a snapshot of the critical steps needed to achieve excellent results.

Quality Matters – SEC Analysis For Antibody Aggregates

Size exclusion chromatography is the go-to analytical method for therapeutic protein drugs. This article describes the factors affecting the reproducibility of columns and how you can minimize column variation.

High-Loaded Dosage Forms: Novel Platform Expands Dispersion Utility

Spray-dried amorphous solid dispersions (ASDs) show enormous promise in the delivery of drug compounds with low solubility. A novel platform expands the utility of this approach to meet patient needs.

What’s The Best Path For Your Low Soluble Molecule? – Infographic

A tale of two molecules, both designed to treat the same condition, both with solubility challenges. Two biopharma companies racing to be first.

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