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In the News

Drug Discovery & Development (May 2024)

How much does a clinical research associate impact a company’s carbon footprint? More than you might think!

Michael Cohen discusses the need to better understand our respective carbon footprints and develop solutions to reduce the environmental impact of clinical trials.

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BioSpectrum Asia (April 2024)

What’s APAC’s Recipe of Success in Clinical Trials Market?

Ding Ming talks about the ongoing efforts foster an environment that is more conducive to clinical trials.

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Drug Discovery & Development (April 2024)

Real-world evidence key to navigating new policy changes

Evidera’s Ariel Berger and Almudena Olid Gonzalez discuss the expanding role of real-world evidence in drug development.

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Applied Clinical Trials (April 2024)

Unleashing Their Potential: The Evolving Landscape of DHTs

Jill Sommerville, Lauren Flood and Matthew Ryan outline key considerations in deploying fit-for-purpose digital health technologies in drug development.

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CenterWatch Monthly (April 2024)

Cracking the talent shortfall: Strategies for delivering the right talent with an FSP model

Jason Tate lays out multiple approaches to weathering clinical research workforce constraints through the use of FSPs.

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Drug Development & Delivery (April 2024)

Therapeutic Vaccines Development: At the Edge of a New Revolution

Our subject matter experts discuss advances in therapeutic vaccines development for the prevention of infectious diseases.

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American Pharmaceutical Review (March 2024)

Use of AUC in AAV Analysis in a GMP Setting

Jie Ding and Jurgen Hannig discuss how to address shortcomings in software that does not comply with GMP standards.

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EBR (March 2024)

Bridging therapeutic areas in the evolving metabolic space: opportunities, challenges and future perspectives

Graham Ellis, executive senior director, provides an overview of important developments happening in the diabetes/obesity/metabolic space.

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Drug Discovery & Development (March 2024)

Moving the needle on diversity in clinical trials: Where do we go from here?

Rose Blackburne discusses the latest regulatory requirements around diversity in clinical trials, how the industry is responding and what actions will help enable further progress in clinical trial health equity.

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