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Curcuminoids extracted from Curcuma longa have established themselves as prominent compounds in globally integrated wellness formulations. Historically recognized for their strong biological properties, these active components are highly sought after by global health supplement brands and pharmaceutical entities alike. However, delivering curcumin in an bioavailable form remains a persistent challenge in nutraceutical manufacturing.
As a premier CE Certified Curcuma Capsule Manufacturer, our facility addresses this critical issue. We utilize premium-grade, highly concentrated raw ingredients, combined with advanced encapsulation technologies. Our manufacturing methodology ensures that each capsule contains precise, standardized doses of active curcuminoids. Furthermore, our products adhere strictly to rigorous international safety parameters, establishing Chengdu Chenlv Herb Co., Ltd. as an industry-leading global manufacturing partner.
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Providing high-purity, standardized active ingredients that meet strict global regulatory frameworks.
Each batch of our Curcuma capsules is standardized to contain a minimum of 95% total Curcuminoids. This profile includes Curcumin, Demethoxycurcumin, and Bisdemethoxycurcumin, verified by advanced High-Performance Liquid Chromatography (HPLC).
To overcome low absorption barriers, we specialize in custom formulations that combine Curcuma extract with natural absorption enhancers, such as standard Piperine (Black Pepper Extract), which increases absorption rates up to 2000%.
We provide both HPMC (hydroxypropyl methylcellulose) vegetarian capsules and traditional bovine gelatin options. Our capsules are completely free from synthetic binders, artificial colorants, and genetically modified organisms (GMOs).
Established in 2012, Chengdu Chenlv Herb Co., Ltd. has developed into a high-tech enterprise specializing in the research, development, production, and distribution of botanical extracts and active pharmaceutical ingredients (APIs). Our primary focus is on delivering natural raw materials that prioritize safety and efficacy.
Operating from a state-of-the-art 2,711 m² extraction facility in southwest China, we process and refine raw botanicals to supply partners in the supplement, pharmaceutical, cosmetic, and animal nutrition sectors. Our team utilizes advanced extraction systems to support custom formulations, and our products are currently distributed across international markets.
How we leverage agricultural resources, manufacturing facilities, and compliance frameworks to support global distribution.
Located in Sichuan Province, our facility has direct access to diverse botanical resources. This enables us to monitor agricultural inputs closely, verify quality at the source, and control logistics costs effectively.
We use automated counter-current extraction systems and membrane separation technologies. These processes maximize the yield of active compounds while keeping energy consumption low.
Every product batch is accompanied by a comprehensive Certificate of Analysis (CoA). Testing includes HPLC purity validation, heavy metal limits (Pb, As, Hg, Cd), pesticide residue screens, and microbiological assays.
We provide contract manufacturing services ranging from custom ingredient blending and specific capsule sizes to bulk supply, white-label packaging, and export logistics.
Adapting botanical materials to meet the regulatory, cultural, and environmental demands of local markets.
Our Curcuma capsules are designed to comply with EU Regulation 396/2005 for pesticide residues, standard limits for Polycyclic Aromatic Hydrocarbons (PAHs), and the strict prohibition of Ethylene Oxide (EtO) treatment. The CE mark validates our adherence to these requirements.
We support global registration processes by providing complete technical documentation. This includes DMF (Drug Master Files) support, stability data, allergen declarations, non-GMO statements, and BSE/TSE-free certifications.
Our logistics team handles international customs clearance procedures. We prepare documentation for key regulatory systems, including REACH in Europe, FDA import requirements in the US, and target clearances across APAC markets.
Supplying botanical extracts tailored to the performance and formulation needs of diverse industries.
We supply standardized ingredients for joint health formulations, natural antioxidant blends, and products supporting digestive and cardiovascular health.
Our high-purity extracts serve as active ingredients in integrative medical formulas, therapeutic preparations, and standardized herbal remedies.
We process natural ingredients for skincare formulations targeting antioxidant properties, soothing properties, and anti-aging applications.
We provide natural feed additives designed to support immune function, digestion, and general health in livestock and aquaculture systems.
From initial design to global delivery, we offer a transparent, standardized contract manufacturing process.
We work with clients to define product parameters, active compound levels, capsule options, and target packaging requirements.
Our team develops a detailed quotation based on current raw material costs, processing requirements, order volume, and packaging configurations.
We establish a formal contract defining delivery terms, quality standards, regulatory compliance, and confidentiality requirements.
Our lab produces prototype batches for quality checks, analytical testing, and active level confirmation prior to full production.
Once samples are approved, our GMP-compliant facility begins full production, utilizing automated encapsulation and quality controls.
Each batch undergoes testing for purity, heavy metals, microbial limits, and capsule consistency, accompanied by a final Certificate of Analysis.
Finished products are packed and shipped using temperature-controlled logistics, with all necessary export documents included.
Our manufacturing processes are verified under recognized international standard frameworks.
Key information regarding botanical material pricing, seasonal crops, and global supply dynamics.
Recent shifts in major agricultural regions, such as pricing adjustments for Citrus aurantium, reflect supply fluctuations driven by seasonal yields and rising processing costs. We maintain buffer stocks to protect clients from sudden market pricing shifts.
We join global pharmaceutical and nutraceutical partners at trade events like CPHI China. These exhibitions support the development of active ingredient technologies and help address regulatory changes in the international supply chain.
Recent developments in plant extraction focus on eco-friendly solvents and improved bioavailability. Chengdu Chenlv Herb invests in ongoing process development to support active ingredient consistency.
Key information regarding technical specifications, testing protocols, and customization options.
We analyze active curcuminoids (curcumin, demethoxycurcumin, and bisdemethoxycurcumin) using High-Performance Liquid Chromatography (HPLC). Standard specification assays are verified by third-party testing services (such as SGS or Eurofins) to ensure compliance with label claims.
We prioritize food-grade ethanol and purified water for extraction. Solvents such as ethyl acetate, hexane, or methanol are excluded. Gas Chromatography-Mass Spectrometry (GC-MS) testing is conducted on every batch to verify that residual solvents remain below EU and USP pharmacopoeia limits.
The CE marking verifies that our products comply with European health, safety, and environmental protection regulations. It indicates that the raw materials, manufacturing practices, capsule shells, and packaging meet European standards for dietary supplements.
Yes. We offer customization for capsule size (e.g., Size 00, 0, or 1), dosage levels (typically 250mg to 750mg), and blended formulations. Popular blends include Curcumin combined with Piperine, Ginger, or Boswellia Serrata extract.
Every raw material batch undergoes Inductively Coupled Plasma Mass Spectrometry (ICP-MS) testing for heavy metals (Lead < 3.0 ppm, Cadmium < 1.0 ppm, Mercury < 0.1 ppm, Arsenic < 1.0 ppm). We screen for PAHs and pesticide residues using gas chromatography (GC-MS/MS) to meet strict EU limits.
For custom ODM/OEM formulations, production is typically completed within 3 to 4 weeks after sample validation and design approval. Standard bulk powder orders are processed and shipped within 7 to 10 working days.
Standardized botanicals and specialized ingredients for diverse international regulatory regions.
