Newsletter | December 15, 2020

12.15.20 -- Researchers Target Thyroid Cancer With Triple Threat Drug Combination

Industry Insights
Lipid-Based Formulations For Early-Stage Clinical Trials

For certain molecules, the most appropriate technology for bioavailability enhancement and accelerated development will be lipid-based formulations (LBF), supported by in silico development tools. Senior Formulation and Product Development Scientists analyze the potential benefits and applications of lipid/liquid-based formulations and how they may reduce timelines to clinical trials.

Quantification Of Vector Genomic DNA And Residual DNA In Gene Therapy Vectors Using ddPCR

Bringing cell and gene therapy drugs to market requires improvement in many areas, including analytical testing methods, which are used to determine the safety, strength, and purity of viral vectors.

Cost Savings And Speed: The Untapped Value Of A Single-Source Solution

Small and emerging companies face significant challenges in today’s market. This calls for an alternative solution to help them achieve success.

The Path To High-Quality Immunoassay Reagents

There is a continued demand for novel, fit-for-purpose immunoassays. It’s important for developers to streamline the selection and potential modification of critical reagents to get tests to market quicker.

Multiplexing: Managing Risk With Proven, Single-Use Solutions

Typically, demand forecasts for drugs prior to launch reflect a huge range of expectations. This illustrates just how hard it is to forecast accurately. Instead of trying to make better predictions (which will never be wholly accurate nor truly able to remove risk), or erring on the side of overcapacity (which is a drag on ROC), developers and CDMOs should seek manufacturing flexibility.

From Molecule To Medicine. Delivered.

To be able to meet the growing needs of patients around the world, a company must have a strategy that can shepherd new biologic therapies throughout the development timeline.

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