Newsletter | June 13, 2025

06.13.25 -- Reactive To Proactive: A Major Shift In The Fight Against Alzheimer's

NEW PODCAST EPISODE

The Discovery Of Microbes And Implications For Public Health Today, With Science Writer Thomas Levenson

On Business of Biotech, Thomas Levenson, MIT professor and author of So Very Small: How Humans Discovered The Microcosmos, Defeated Germs — And May Still Lose The War Against Infectious Disease talks about what he learned in the writing of So Very Small, how cultural and political forces shape scientific progress, and what it means for drug developers, public health officials, and patients everywhere. Brought to you by Avantor.

FEATURED ARTICLE

Reactive To Proactive: A Major Shift In The Fight Against Alzheimer's

Improvements in diagnostics for the early detection of Alzheimer's disease have the potential to transform patient care and new drug development, writes Mike Banville, CEO and President at ALZpath.

INDUSTRY INSIGHTS

Improving The Patient Experience In Clinical Research

To preserve the quality of care and build a more effective approach to trial design, a sponsor must consider their approach to patient recruitment and enrollment early and often.

PTRME Founders' Journey Focuses On Entrepreneurs In 'Fireside Chat'

Learn more about a major workshop intended to empower biotech innovators with tools, mentorship, and connections to accelerate regenerative medicine breakthroughs from research to real-world impact.

3D Screen Printing: Enabling A New Generation Of Complex Formulations

Screen-Printed Innovative Drug Technology can produce oral, transdermal, and implantable dosage forms while ensuring heterogeneous distribution of active ingredients.

The Top 5 Myths About eCOAs In 2025

Join leading clinical experts as they debunk the top myths about eCOA in 2025, separating fact from fiction to help clinical operations, procurement, and data management teams make smarter decisions.

How To Establish Effective, Scalable Drug Safety Ops Across Vendors

Numerous factors impact a drug safety program, but proper management of three key elements drives success while creating a scalable drug safety model.

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