Demystifying Enzymatic Synthesis: Why It's the Gold Standard for Injectable-Grade NAD+? The NAD+ therapy market is booming, but the choice of manufacturing process directly dictates the upper limit of product safety and efficacy. ⚗️ Chemical synthesis involves complex pathways, easily introducing unknown impurities and organic solvent residues, posing potential risks for IV injection. In contrast, Enzymatic Biocatalysis, adopted by Howa Biotech, mimics the natural in-vivo synthesis pathway and offers unparalleled advantages: ✅ Ultra-High Purity: Achieves ≥99% main purity effortlessly with a clear and controllable impurity profile. ✅ Extremely Low Endotoxin: Consistently controlled at <0.2 EU/mg, far exceeding injectable-grade standards. ✅ High Bioactivity: Correct spatial structure ensures biological function. For pharmaceutical companies and high-end clinics, choosing a raw material supplier is choosing a risk-control partner. Advanced technology is the first line of defense for safety. sales@horwats.com +86 19052754932(whatsapp) #NAD #IVTherapy #Biotechnology #cGMP #EnzymaticSynthesis

Hollywood IV Trend (Business Insider) 💉 From Beverly Hills to New York, celebrities are lining up for NAD⁺ drips. But the difference between a fad and a medical solution is purity. Only pharma-grade NAD⁺ meets the standards for IV and compounding use. That’s why Horwats supplies clinics with COA-backed NAD⁺, optimized for rapid solubility and low endotoxin. sales@horwats.com +86 19052754932(whatsapp) #IVTherapy #NADplus #Horwats