Understanding Nootropics with TSI Group

Understanding Nootropics with TSI Group

The company’s enfinity paraxanthine and PEAK ATP are stirring up the market for cognitive health enhancement.  Nootropics have continued to gain in popularity. In this episode, learn what nootropics are, why there’s so much attention on cognitive health and mental energy, and TSI Group’s branded ingredient solutions: enfinity paraxanthine and PEAK ATP.  Shawn Baier, VP of Business Development at TSI Group discusses the health benefits, clinical evidence, formulations, stim vs non-stim energy, and more.

Bionap Discusses Ingredient Sourcing, Science, and Sustainability

The vertically integrated supplier offers a range of standardized extracts derived from plants indigenous to the Mediterranean basin. In this podcast, Violetta Insolia, Business Development Manager at Bionap, discussed scientific collaborations the company has entered with universities around the world to validate its ingredients. Most recently, the company has launched ODILIA, a powder extract obtained from Opuntia cladode juice standardized in polysaccharides and piscidic acid. Insolia discussed the Bionap’s approach to innovation and R&D, and reviewed the company’s commitment to sustainability and upcycling.

NAD+ and Aging: ChromaDex CEO Rob Fried Discusses Science, Industry Challenges and Future Expectations

With rising interest in healthy aging, more people are looking for clinical research that supports products designed to help them live healthier for longer. The coenzyme NAD+ is essential to the body's metabolic processes, but it declines with age, so supplements that boost NAD+ have garnered considerable attention in the scientific community. ChromaDex, which is publicly traded on the Nasdaq, offers the consumer product brand Tru Niagen. This patented form of nicotinamide riboside (NR) is a precursor to NAD+. Tru Niagen sales totaled nearly $70 million last year, accounting for the majority of the company’s $83.6 million in revenue. In this interview, ChromaDex CEO Rob Fried discusses NAD+ and emerging research, the company’s evolution to become a consumer-focused nutraceutical, the future of aging, critical challenges in today’s dietary supplement market, and more. Spoiler alert: Fried is calling for more accountability and collaboration to enforce quality standards and establish greater trust with consumers. In addition to being CEO of ChromaDex [https://www.chromadex.com/] since 2017 and the founder of Tru Niagen [https://www.truniagen.com/], Fried is an Academy Award and Emmy Award winning motion picture producer [https://www.imdb.com/name/nm0294975/awards/]. Before his combined 7 years in the health industry, he held senior roles at entertainment companies Savoy Pictures (CEO), Columbia Pictures (Executive Vice President) and Fried Films (founder, CEO). He has also founded and served as CEO of internet companies Feeln (now Hallmark Movies Now), WHN (a leading e-commerce service provider), and Healthspan Research LLC.  In 2017, Fried led ChromaDex’s acquisition of Healthspan Research LLC, a consumer company offering Tru Niagen products, and raised funds with Horizon Ventures to offer Tru Niagen direct-to-consumer. He holds a BS from Cornell University and an MBA from the Columbia University Graduate School of Business.

What Does FDA’s Reorganization Mean for the Dietary Supplement Industry?

Loren Israelsen from the United Natural Products Alliance shares insight on how agency priorities might change and how businesses can prepare. The U.S. Food and Drug Administration is in process of a massive reorganization designed to streamline operations within a unified Human Foods Program [https://www.fda.gov/about-fda/fda-organization/fdas-proposal-unified-human-foods-program-and-new-model-office-regulatory-affairs] (HFP) to largely replace the Center for Food Safety and Applied Nutrition (CFSAN). What does this mean for the dietary supplement industry? In the proposal, now under review at Health and Human Services (HHS), the Office of Dietary Supplement Programs (ODSP) will report to a newly created “Office of Food Chemical Safety, Dietary Supplements, and Innovation,” (OFCSDSI), which FDA said “will work to modernize and strengthen oversight of food chemical safety, advance dietary supplement safety, and enable the Human Foods Program to support and effectively regulate food ingredient innovation.” As the agency’s first Deputy Commissioner of Human Foods, Jim Jones [https://www.nutraceuticalsworld.com/contents/view_breaking-news/2023-08-24/fda-names-deputy-commissioner-for-proposed-human-foods-program/] is a 30-year veteran of the Environmental Protection Agency (EPA) with a deep background in chemical safety. Jones and his staff met last December with several major trade associations representing the supplements industry, including Loren Israelsen, founder and president of the United Natural Products Alliance. I talked with Loren recently about FDA’s restructuring and how priorities might change under an overhauled Human Foods Program with new leadership. — Sean Moloughney, Editor, Nutraceuticals World, nutraceuticals@rodmanmedia.com [nutraceuticals@rodmanmedia.com]

Radicle Science Aims ‘Proof-as-a-Service’ Model Toward Predictive Nutrition

One of the biggest challenges for dietary supplements has been proving that products actually work.    The traditional model for clinical research is expensive, slow, and not representative of diverse populations. As its name suggests, the company Radicle Science aims to address those concerns with a much different approach, leveraging new tools and technology.     For this podcast we talked with founders Pelin Thorogood, executive chairwoman, and Dr. Jeff Chen, CEO, to learn more about their work and overall mission.    If you’d like to offer feedback or suggest a topic, you can email us at Nutraceuticals@RodmanMedia.com [Nutraceuticals@RodmanMedia.com]