Since 2018, Shaanxi Bieyouth Biotech Co., Ltd. has redefined the standards of a Health Care Product Manufacturer & Supplier. With a deep integration of scientific research and industrial-scale production, we provide an information gain advantage by focusing on high-purity extraction and bioactive stability.
Our GMP-certified facilities house two standardized workshops equipped with precision extraction technology. We don't just supply raw materials; we engineer solutions for the dietary supplement, cosmetic, and pharmaceutical sectors, ensuring every milligram of NMN, Glabridin, or Coenzyme Q10 meets rigorous analytical benchmarks.
Exporting to the USA, UK, Canada, Russia, and Australia, we are recognized as a "large-scale gold supplier." Our authority is backed by FDA certification (2023) and a history of integrity in international trade.
In the post-pandemic era, procurement directors prioritize resilience and transparency. Our Shaanxi-based facility represents the peak of "Factory 4.0" in the biotech space. We leverage IoT-enabled monitoring of extraction temperatures and automated packaging systems to minimize human error.
Transitioning toward solvent-free extraction methods to meet the "Clean Label" demand. This ensures zero residue in delicate compounds like Centella Asiatica and Epitalon.
Integrating fermentation-based production for rare cannabinoids and high-purity NMN to reduce environmental footprint while increasing bioavailability.
Developing predictive models to determine how plant extracts interact within complex dietary supplement matrices, improving the shelf-life stability of products like Glabridin and Allulose.
Providing high-purity powders (Coenzyme Q10, L-Arginine) for capsules and tablets focusing on heart health and longevity.
Active ingredients like Retinol and Hydrolyzed Sponge for skin metabolic repair, anti-aging, and acne treatment formulations.
Sugar substitutes (Allulose) and natural colorants (Butterfly Pea Flower) that meet FDA GRAS standards for healthy lifestyle branding.
Standardized extracts used as precursors for advanced drug development in respiratory and anti-fatigue therapies.
Navigating the regulatory landscape is the biggest hurdle for global procurement. At Bieyouth Biotech, we provide comprehensive documentation support including MSDS, COA, TDS, and Third-Party Lab Reports.
Our localization support ensures that whether you are in the EU following EFSA guidelines or in the US following DSHEA, our ingredients are ready for seamless integration. We offer Private Label Packaging tailored to local market languages and design preferences.
Defining product specifications, active concentration (e.g., Oat Beta Glucan 80%), and target demographics.
Prototype development in our Institute of Biology to verify efficacy and sensory profiles.
Scalable manufacturing in GMP workshops with real-time quality monitoring.
Customs-ready shipping with optimized logistics to North America, Europe, and Asia-Pacific.
Our production facilities are GMP certified, and we hold an official FDA registration. We provide COA (Certificate of Analysis) for every batch to ensure purity and potency.
Yes, we specialize in OEM/ODM. Whether you need Centella Asiatica at 99% or a custom blend of Anserine for joint support, our lab can tailor the specifications to your formulation needs.
For standard raw materials in stock, lead time is 3-5 days. For custom OEM formulations or private labeling, lead times vary from 14 to 21 days depending on packaging requirements.
We use vacuum-sealed, multi-layer UV-protected packaging. For sensitive compounds like NMN or Retinol, we utilize temperature-controlled logistics options to maintain integrity.
Bieyouth
