In this special episode of the Xtalks Life Science Podcast, part of our Breakthrough with Dr. Corey Stanton series, host Dr. Corey Stanton speaks with Neal Dunkinson, Sr. Director of Solution Sales at Copyright Clearance Center (CCC), about why copyright and licensing are becoming mission-critical in modern life sciences research, particularly in the era of AI.

Life sciences teams both generate and consume vast amounts of scientific literature, clinical data and third-party content. As Neal explains, copyright and licensing are no longer back-office considerations; they are central to enabling compliant collaboration, reducing information silos and supporting confident decision-making across R&D, medical affairs and regulatory teams.

In this episode, Neal discusses the most common challenges organizations face when managing scientific literature and internal knowledge workflows, and how those challenges evolve as companies grow from early-stage biotechs into global enterprises. He highlights where compliance risks and information silos typically emerge in real-world research environments and how structured licensing strategies can help mitigate them.

The conversation also explores how CCC’s approach to “making copyright work” translates into practical value for scientists and knowledge workers: removing friction from access to content while ensuring proper rights management behind the scenes.

As AI-driven analytics and generative tools become embedded in life sciences workflows, new copyright considerations are emerging. Neal explains how CCC supports responsible AI development by enabling lawful access to high-quality content while ensuring that publishers and creators are fairly compensated. He shares his perspective on what “responsible AI” means in scientific research and how licensing frameworks will likely evolve as AI adoption accelerates.

Neal joined CCC in January 2025 and brings 20 years of experience in informatics solutions for the life sciences R&D market. Over the course of his career, he has held roles at Thomson Reuters, Accelrys/Biovia and SciBite/Elsevier, where he helped scale SciBite from a four-person startup through its acquisition and integration into Elsevier. At CCC, he focuses on licensing and content workflow solutions tailored to the needs of life sciences organizations, aligning product capabilities with complex research and compliance requirements.

Tune in to learn how forward-looking content and licensing strategies can help life sciences organizations future-proof their research operations while advancing compliant, AI-enabled discovery.

For more life science and medical device content, visit the Xtalks Vitals homepage. https://xtalks.com/vitals/

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In this week’s episode of the Xtalks Life Science Podcast, host Ayesha Rashid, Senior Life Science Journalist at Xtalks, spoke with Dave Rosa, CEO, NeuroOne Medical Technologies Corporation, a company developing minimally invasive diagnostic and therapeutic electrodes employed in nerve ablation as well as neuromodulation devices to treat conditions such as epilepsy and chronic pain and enable drug delivery into the brain.

Mr. Rosa is an entrepreneur with three decades of experience in the medical device industry spanning a variety of technologies and products. In addition to CEO roles with early-stage medical device companies, Mr. Rosa’s background also includes senior roles with C.R. Bard Inc., Boston Scientific Inc. and St. Jude Medical, where his responsibilities included marketing, product development and business development. He has been named as an inventor on multiple medical device patents, serves on seven corporate boards and has raised more than $200M in the capital markets.

Mr. Rosa holds an MBA from Duquesne University and a Bachelor of Science (BSc) in Commerce and Engineering from Drexel University.

Tune in to learn about advancements in neuromodulation and nerve ablation for chronic pain.

For more life science and medical device content, visit the Xtalks Vitals homepage. https://xtalks.com/vitals/

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In this week’s episode of the Xtalks Life Science Podcast, host Ayesha Rashid, Senior Life Science Journalist at Xtalks, spoke with Kevin Caldwell, CEO, Co-Founder & President of Ossium Health, a biotechnology company advancing the first off-the-shelf bone marrow therapy derived from deceased organ donors. The treatment is designed to address longstanding clinical and logistical challenges in allogeneic bone marrow transplantation.

Kevin Caldwell has led Ossium Health in building more than 50 strategic partnerships with biopharmaceutical companies and helped secure a transformative federal contract with BARDA (Biomedical Advanced Research and Development Authority).

Prior to founding Ossium, Kevin served as an Engagement Manager at McKinsey’s San Francisco office where he advised clients in the biotechnology and healthcare sectors, and prior to that, served as a Senior Investment Associate at Bridgewater Associates where he did quantitative research for the firm’s global macro investments. Kevin holds degrees in Physics and Economics from MIT and a JD from Harvard Law School.

Tune in to learn about how about the landscape of cell therapy and allogeneic transplantation, including the translation of off-the-shelf cellular therapies into clinical practice and how emerging models could reshape bone marrow transplantation workflows.

For more life science and medical device content, visit the Xtalks Vitals homepage. https://xtalks.com/vitals/

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