In this episode, Dr. Bharathi B, from Natural Remedies, discusses the science behind Ashwa.30™, a next-generation, bioactive-optimized ashwagandha extract formulated to deliver clinical efficacy at just 30 mg per day. She explains how its dual standardization to withanolides and a proprietary ATP-active fraction broadens adaptogenic support beyond conventional extracts, and how human clinical trials, metabolomic insights, and biomarker data support its role in promoting cellular health for healthy ageing and longevity.
Ixoreal Biomed highlights an exploratory placebo-controlled study of SRI-81 Shatavari, alone and combined with KSM-66 Ashwagandha, published in the International Journal of Women’s Health.
Clinical research moves beyond compliance, focusing on smarter trial design, risk-based quality, and “evidence engineering” to deliver decisive, decision-ready results.
Horphag Research's Sébastien Bornet breaks down the clinical science behind Robuvit, exploring how the caffeine-free French oak extract supports mitochondrial energy, mood stability, and stress resilience.
Todd Harrison, co-chair of the FDA practice group at Venable LLP, explains how California’s AB 2779 changes date-labeling requirements for supplements, why stability testing matters, and how companies can navigate evolving state rules while advocating for federal uniformity.