- Custom Formulation Programme — All Applications
Can't find what you need in our catalogue?
We'll build it for you.
Our public catalogue represents less than 20% of what we can manufacture. With over 300 botanical species, 5 extract formats, and a fully equipped in-house analytical laboratory, we develop pharmaceutical-grade botanical extracts to your exact specification — for nutraceuticals, cosmetics, veterinary, food, and pharmaceutical applications alike.
"If the plant exists and the active compound can be standardised, we will find a way to extract it, verify it, and deliver it — freshly produced, batch-dated, and fully documented."
— Founder
300+
Botanical species
in active R&D library
6
Application sectors
nutra · cosmo · vet · food · pharma · more
24mo
Retained samples & stability
for every custom batch
Active marker & potency target
Custom standardisation (e.g. Forsythia extract with Phillyrin ≥ 6%, Astragalus Polysaccharides ≥ 60%) validated by HPLC or UV, matched to your application and market.
Physical form & solubility profile
Dry powder, fluid extract, water-soluble granule, botanical oil/oleoresin, or compound multi-herb formula — each optimised for your end formulation
Regulatory grade & documentation
GMP CoA, heavy metal panel, pesticide residue, solvent residue, stability data — documentation package matched to your target market (EU, US FDA, China NMPA, ASEAN)
Freshness & production date
Every batch is produced to order — not drawn from warehouse stock. The manufacturing date on your CoA reflects real production, not inventory that has been sitting for 12 months
Packaging & private label
Drum, bag, or small SKU; private-label available under NDA
The problems
procurement teams face — and
how we solve them.
We have heard every objection. Below are the six most common barriers buyers encounter when sourcing custom botanical extracts — regardless of whether the application is nutraceutical, cosmetic, veterinary, food, or pharmaceutical.
"I can't find the specific herb or specification I need."
Standard catalogues are commercial decisions, not botanical limitations. Most suppliers list only their highest-volume SKUs. If your target herb or potency level isn’t shown, that doesn’t mean it can’t be made.
Our answer:
Our internal R&D library covers 300+ botanical species spanning nutraceutical, cosmetic, veterinary, and pharmaceutical applications. If the plant is pharmacopoeially documented and the active compound is measurable, we develop a validated extraction process for it. Tell us the plant name and the active marker you need — we assess feasibility within 48 hours, free of charge.
"I receive product with an old manufacturing date and questionable freshness."
A common frustration across all sectors: the extract you ordered was produced 9–18 months ago, pulled from slow-moving inventory. Active compound levels have already begun to drift — before you even open the drum.
Our answer:
Every custom order triggers a dedicated production run. We do not fill custom orders from pre-existing warehouse stock. The manufacturing date on your CoA is the date we produced it — typically within the 4 weeks preceding dispatch. You receive a genuinely fresh batch, with full potency intact.
"The lead time for custom development is too long for our launch timeline."
Many manufacturers treat custom work as a back-office project with no defined milestones or committed delivery dates. Buyers are left chasing updates while their launch window closes.
Our answer:
We use an agile 3-phase process with fast stage gates: lab-scale feasibility (3–5 days), pilot-batch validation (1–2 weeks), and accelerated commercial production. You receive a precise timeline at the start of each phase. For herbs readily available at our facility, custom lab samples can be extracted, tested, and shipped in as few as 3 business days.
"I'm worried about formula confidentiality."
A proprietary formulation or novel extraction specification represents significant R&D investment. The risk of a supplier reverse-engineering or reselling your formula to a competitor is a legitimate concern across every industry.
Our answer:
We provide a mutual NDA before any formula details are discussed — not after. Our custom formulation contracts include explicit IP ownership clauses confirming that your formula, specification, and process parameters remain your exclusive property. We do not sell formulas derived from client briefs to third parties, period.
"I'm not sure the product will remain consistent batch to batch."
Natural botanical extracts are inherently variable. Buyers who have been burned by inconsistent potency, colour shifts, or solubility changes between batches need more than a supplier’s verbal assurance.
Our answer:
Every custom product is validated with an in-house master specification and a validated HPLC or UV analytical method. All batches are tested against that specification before dispatch. We run real-time and accelerated stability studies and retain 24-month samples from every batch — so if a potency question arises 18 months after delivery, we can retest the retained sample within 5 business days.
"Can you scale up from a small sample to full production?"
Many manufacturers can produce a convincing 100 g lab sample but lack the extraction infrastructure to maintain that quality at multi-hundred-kilogram scale. Buyers discover this only after committing to a launch.
Our answer:
We bridge the gap between lab formulation and mass production. Our core facility in Lushi covers 23,000 m² of production space, powered by a heavy-duty line of six 6-ton extraction tanks. Our pilot-batch phase (200–500 kg) specifically exists to de-risk this transition. We never release a commercial specification until pilot data proves the process is stable and scalable.
A purpose-built botanical extract manufacturer. Built for the rigour every application demands.
Many extract suppliers operate as general chemical processors or food-grade blenders who have added a botanical line to their catalogue. The consequence is inconsistent quality standards, shared production equipment, and documentation systems designed for low-risk ingredients rather than regulated products.
Was established specifically to manufacture high-specification botanical extracts for regulated industries — nutraceuticals, cosmetics, veterinary, food, and pharmaceutical markets. Our facility, documentation systems, and QA protocols are designed around the most demanding regulatory requirements from the ground up.
We are located in Lushi, China — a core region renowned for its authentic medicinal herbs. Our proximity to raw material sources, particularly for premium Forsythia and other regional botanical species, gives us supply chain transparency and quality control from the very source that coastal manufacturers cannot match.
We currently supply formulators, brand owners, and pharmaceutical manufacturers in 18 countries, including Germany, the Netherlands, the United States, Australia, Thailand, Vietnam, and Brazil. Each market presents different regulatory requirements, and our documentation team is experienced in preparing export dossiers for EU, US FDA, and ASEAN submissions.
01
Extraction & Concentration
Ethanol and conventional extraction powered by our core line of six multi-function extraction tanks. Downstream processing features single-effect external circulation concentration , precise alcohol precipitation , and fluid-bed drying. We process both single-herb and complex multi-herb compounds. Final standardisation is achieved through validated two-dimensional blending and precision milling.
02
Analytical Laboratory
In-house HPLC and UV-Vis spectrophotometry for precise active compound quantification. Heavy metal testing is strictly controlled via Atomic Absorption Spectrophotometry (AAS) , supported by 1/100,000 precision analytical balances and a full microbiological testing suite. We do not outsource critical potency testing for custom products — your actual measured values are generated directly on our instruments by our own analysts.
03
Stability & Retention Programme
Real-time stability chambers (25°C/60% RH, 30°C/65% RH, 40°C/75% RH) and accelerated testing per ICH Q1A guidelines. 24-month retained samples stored under controlled conditions for every production batch, custom or standard.
04
Documentation & Regulatory Support
GMP batch records, full CoA with actual measured values, raw material traceability, process validation reports, and method validation summaries according to pharmacopoeial standards. Export documentation is optimized for international regulatory submissions and seamless customs clearance.
23,000 m²
Dedicated botanical extract production floor with segregated product streams
300+
Botanical species validated in our R&D extraction library across all applications
45 Tons
Total batch extraction capacity powered by our heavy-duty multi-function tanks.
48 Hrs
Feasibility assessment and lab sample dispatch for cataloged botanical species.
Science-backed development
not guesswork.
Our extraction development programme is supported by active research collaborations with leading Chinese universities and state botanical research institutes. When you ask us to develop a novel extract, you are not relying on a factory technician improvising in the lab — you are drawing on a network of academic phytochemists who have published on the very compounds you are targeting.
The challenge with developing a custom botanical extract is that extraction science is genuinely complex. Yield, selectivity, and reproducibility are all influenced by dozens of interacting variables — solvent polarity, temperature, pH, particle size, extraction time, and the unique phytochemical matrix of each plant. Getting this right for a new compound requires published phytochemical data, validated analytical methods, and the ability to interpret results rather than simply follow a protocol.
Our partnerships with university botanical science departments give us early access to phytochemical research, validated reference standards, and peer-reviewed analytical methods — the same resources that pharmaceutical companies rely on, made available to our custom development clients.
Henan Agricultural University
Joint development of novel botanical veterinary drugs led by our Chief Expert, Prof. Liang Jianping. The collaboration focuses on the research, clinical trials, and regulatory approval of four new Forsythia-based veterinary formulations.
Lanzhou University
Strategic partnership focusing on the comprehensive utilization of Forsythia (fruit, leaf, and stem). Joint initiatives include active compound purification, high-efficiency extraction technologies, and an active postgraduate training program at the university.
Henan University of Chinese Medicine
Dedicated collaboration on botanical quality standardisation and extraction process optimization. This ensures our full-scale commercial production maintains the highest levels of active marker consistency and regulatory compliance.
22 National Patents
Supported by robust intellectual property, holding 22 national patents (including 4 invention patents), with 17 specifically dedicated to Forsythia extraction technologies.
78 Approved Formulations
Proven regulatory success with 78 official drug production approvals, demonstrating our capability to meet the strictest veterinary and pharmaceutical compliance standards.
#1 National Output
Recognised as the leading producer in the industry, our Forsythia extract production volume officially ranked first nationwide in 2025, ensuring unmatched supply stability.
6 Joint R&D Centers
An expansive academic network encompassing 6 leading universities, driving continuous innovation in botanical extraction from lab-scale feasibility to commercial deployment.
"See the extract before you commit to a commercial order."
Our laboratory sample service allows you to evaluate the actual extract — not a specification on paper — before placing a commercial order. For herbs already in our R&D library, a certified 100 g analytical sample with full CoA can be dispatched in as few as 10 business days from brief approval.
Submit a brief
Herb name, active marker target, application type, and any solvent restrictions. No technical degree required — our team will ask the right questions.
Feasibility assessment
Within 48 hours, we confirm whether the extract is achievable at your target specification and what the development process will involve.
Lab-scale extraction
Our extraction team produces your sample at bench scale (100 g – 500 g), optimising solvent system, extraction time, and concentration method.
Certified sample + full CoA
Your 100 g sample ships with a complete analytical certificate: active content by HPLC/UV, moisture, heavy metals, and microbiological status. This is the same documentation standard as our commercial batches.
Why a fresh lab sample matters
The colour, aroma, solubility, and handling characteristics of a botanical extract cannot be fully communicated by a specification sheet. A fresh lab sample produced specifically for your brief — not a leftover from someone else’s order — lets your formulation team evaluate the material in context before any commercial commitment is made.
Our online catalogue is a starting point, not our limit.
Displaying every product we can manufacture is genuinely not possible. A single botanical species may yield dozens of distinct product variants depending on extraction solvent, marker compound, potency level, physical form, and target application grade. A full product matrix for even 50 species would run to thousands of SKUs — no website can usefully present that.
What we list publicly are our highest-demand, in-stock products — the SKUs where most buyers have standard requirements. If your need is more specific, that doesn’t make it unusual. It makes it a custom brief.
1000+
botanical species currently active in our R&D extraction library.
Only ~60 appear in the public catalogue.
If you do not see your target herb, standardisation level, or product form listed on our website — assume we can make it. Contact us with the botanical name and your application. A feasibility assessment costs nothing.
Immune & Anti-infective
Astragalus, Echinacea, Andrographis, Isatis, Houttuynia…
40+ species
Antioxidant & Anti-ageing
Grape Seed, Rosemary, Green Tea, Pomegranate, Goji…
35+ species
Skin & Cosmetic Actives
Centella, Licorice, Bakuchiol, Sophora, Peony Root…
30+ species
Digestive & Hepatoprotective
Milk Thistle, Dandelion, Atractylodes, Hawthorn, Fennel…
35+ species
Anti-inflammatory & Analgesic
Curcumin, Boswellia, Corydalis, Dipsacus, Eucommia…
30+ species
Adaptogenic & Cognitive
Rhodiola, Ashwagandha, Ginkgo, Panax Ginseng, Bacopa…
28+ species
Reproductive & Hormonal
Dong Quai, Cimicifuga, Vitex, Paeonia, Morinda…
22+ species
Reproductive & Hormonal
Dong Quai, Cimicifuga, Vitex, Paeonia, Morinda…
22+ species
Animal Nutrition & Veterinary
Forsythia, Astragalus, Isatis, Eucommia… Specialized extracts for livestock immunity and feed additives.
Targeted efficacy
Don't see your category?
The above is illustrative, not exhaustive. We work from botanical names, pharmacopoeia references, and published research — not a fixed menu. Send us the herb name and the indication or application you are targeting, and our technical team will advise on feasibility.
Five formats. Every one available for custom specification.
The same botanical can be delivered in dramatically different forms depending on your formulation requirements, application type, and target market. All five formats below are available for custom development projects across all application sectors.
01
Dry Powder Extract
Most concentrated form
Highly concentrated, spray-dried powder derived via water or ethanol extraction, with strictly standardized active markers. Offers excellent flowability and stability. Ideal for human dietary supplements (capsules/tablets) and serves as a premium feed additive base for livestock and aquaculture.
02
Fluid & Soft Extracts
Liquid concentrate
Premium liquid extracts optimized for rapid absorption and seamless formulation. Perfectly suited for cosmetic serums, personal care formulations, and high-purity oral liquid medications for both human and veterinary applications.
03
Soluble Granule
Instant dispersal
Engineered for complete and rapid water solubility without sedimentation. Perfect for human functional beverages and large-scale animal drinking water systems, ensuring zero clogging in automated farm dosing lines.
04
Raw Botanical Powder
Custom 60–500 mesh sizing
Premium botanical materials directly milled to precise particle sizes (60–500 mesh). This mechanical process retains the plant’s natural fiber and full-spectrum profile without extraction. A highly cost-effective solution ideal for human dietary capsules, herbal tea blends, and bulk animal feed premixes.
Compound Multi-Herb Formula
Multi-herb compound formulae require extraction, blending, and standardisation of multiple botanical species in precise ratios. Whether rooted in Traditional Chinese Medicine, Ayurveda, or a proprietary nutraceutical concept, this is our most technically complex service — and our most requested. We handle everything from herb sourcing and ratio optimisation to full analytical validation of the finished compound extract, across any application sector.
Whether you have an existing registered formula that needs a reliable manufacturer, or you are developing a new compound from first principles, our technical team and university R&D partners can take the brief from concept to validated commercial product.
What we need from you
Formula composition (herb list + ratios), target application and indication, intended market and regulatory framework, and any analytical method preferences.
What you receive
Validated extraction protocol, custom analytical methodology to overcome matrix interference, a full CoA with HPLC-verified quantification for the formula's primary active markers, stability data, and complete GMP-compliant production records — on every production run.
IP protection
Your formula is your intellectual property. Mutual NDA signed before any herb names or ratios are shared with our team. Formula ownership explicitly confirmed in writing in every development agreement.
Custom extracts developed for any application, any market.
Our extraction, analytical, and documentation capabilities are designed to serve the specific technical and regulatory requirements of each application sector. The same botanical can require very different specifications, testing panels, and documentation formats depending on where it ends up.
💊
Nutraceuticals & Dietary Supplements
Standardized botanical extracts engineered for premium immune support capsules, daily wellness tablets, and functional powders.
✨
Cosmetics & Personal Care
Ultra-pure fractions and highly refined botanical solutions optimized for premium anti-aging serums, soothing creams, and topical formulations.
🐄
Nutraceuticals & Dietary Supplements
High-potency phytogenic feed additives and natural immune boosters (like Astragalus and Forsythia) designed for intensive livestock farming and pet nutrition.
🍵
Functional Food & Beverage
Completely water-soluble, taste-masked botanical extracts optimized for energy drinks, herbal teas, and RTD (Ready-to-Drink) beverages.
🔬
Pharmaceutical & Botanical Drugs
High-purity botanical active ingredients and rigorously standardized extracts for clinical oral liquids, compound granules, and sterile applications.
🌿
Other & Emerging Applications
Tailored botanical solutions for biopesticides, industrial applications, and academic research requiring precise active marker quantification.
From brief to commercial batch in a structured, transparent process.
Every custom project — whether a single new herb for a cosmetic serum or a complex multi-herb nutraceutical compound — follows the same defined development path. No surprises. No ambiguity. Defined deliverables at every stage before we proceed to the next.
Phase 0 · Intake & Confidentiality — Before we begin
All custom projects start with a confidential intake process. This phase is free of charge and carries no commitment on either side.
NDA Execution
A mutual non-disclosure agreement is signed before any formula details, active marker targets, or proprietary specifications are shared. Typically completed within 24 hours of request.
Technical Brief Review
Our technical team reviews your target herb(s), standardisation requirement, physical form, application type, and target market. A preliminary feasibility assessment is provided within 48 hours. University R&D network consulted for novel or complex compounds.
Quotation & Timeline
Following feasibility confirmation, we issue a written development proposal including fixed-price stages, committed milestone dates, and the complete technical and QC documentation package included at each phase.
Phase 1
Laboratory-Scale Development
Our extraction chemists, supported by academic collaborators where relevant, develop and optimise the extraction process at bench scale (100 g – 2 kg output). The goal of this phase is to establish a validated method that consistently delivers your target active content, physical specification, and application-specific requirements.
- Raw material sourcing and identity verification (TLC, HPLC, macroscopic and organoleptic)
- Solvent system, temperature, and extraction time optimisation for your target active and application grade
- Active marker quantification by HPLC or UV at each optimisation step; university reference standards utilised where available
- Physical characterisation: moisture, mesh size, colour (L*a*b* for cosmetic applications), solubility, flow properties
- 3× replicate extractions to confirm method repeatability and yield consistency
- Deliverable: 100 g certified lab sample with full analytical report — ready for your formulation team to evaluate
Phase 2
Pilot Batch Validation
The validated lab method is transferred to production-scale equipment at 10–50 kg output. This phase exists specifically to identify and resolve any scale-up challenges before commercial commitment. You are not locked into commercial production until pilot-batch data is reviewed and approved by both parties.
- Full GMP documentation: batch manufacturing record, in-process controls, deviation log
- Comprehensive analytical testing: HPLC/UV active content quantification, microbiology, moisture, and any application-specific physical parameters (e.g., colour value, pH, solubility)
- Process parameter confirmation: extraction yield, concentration ratio, drying performance
- Accelerated stability initiation: pilot batch placed into 40°C/75% RH chambers per ICH Q1A
- Deliverable: 200–500 kg pilot batch with full GMP documentation package, CoA, and pilot-batch validation report
Phase 3
Commercial-Scale Production
With a validated pilot process and confirmed commercial specification, we move into full-scale production. Every commercial batch is produced to order — not pre-manufactured and stored. The manufacturing date on your CoA reflects actual production for your order, ensuring you receive genuinely fresh material with full active content integrity.
- Every batch produced fresh for your order — manufacturing date on CoA reflects actual production, not warehouse stock
- Full GMP batch records, in-process testing, and final release testing against your validated master specification
- CoA issued with actual measured values — not specification limits; the number on the certificate is the number we measured
- Retained sample registered in 24-month stability programme at dispatch
- Export documentation: Certificate of Origin, CoA, and applicable Health/Phytosanitary certificates arranged based on your specific destination market regulations
- Ongoing real-time stability testing continues in parallel with commercial supply
Phase 4
24-Month Retention & Stability Programme
This programme provides documented evidence of product stability, a core requirement for most quality system audits. Applied rigorously to initial validation batches and annual representative production runs, the programme ensures your botanical extracts maintain full active integrity and physical consistency throughout their stated shelf life.
- Retained sample: A representative sample from every batch is sealed and stored under ICH-recommended conditions (15–25°C, humidity-controlled, light-protected) for 24 months
- Real-time monitoring: Routine active content and physical status evaluation at critical shelf-life intervals (e.g., 6, 12, and 24 months)
- Accelerated stability: Pilot batch and first commercial batch tested at 40°C/75% RH per ICH Q1A for early shelf-life prediction
- On-demand retesting: Retained sample retesting within 5 business days on request, at any point within the 24-month window
- Stability report: Full summary reports at 6, 12, and 24 months, formatted for regulatory dossier submission in your target market
The same analytical rigour
we apply to standard products —
applied to yours.
Custom does not mean less documented. Every custom extract we produce is held to the same GMP standards and analytical requirements as our catalogue products. In many cases, the documentation is more extensive — because a custom product requires a validated method that didn’t exist before we developed it.
Validated Analytical Method
Active markers in every custom product are rigorously quantified using our in-house High-Performance Liquid Chromatography (HPLC) and UV-Vis systems. We develop fit-for-purpose analytical methods, referencing university-published research where available. Validation includes specificity, linearity, accuracy, and precision per ICH Q2(R1) guidelines. The complete HPLC methodology is documented and made available to your QA team.
Certificate of Analysis — Actual Values, Fresh Data
Our CoA reports the value actually measured on the batch you receive, not a specification limit. If HPLC shows 73.4% active content, the CoA states 73.4% — not "≥ 70%". Furthermore, the testing date on your CoA is within weeks of dispatch — not months-old data applied to aged stock. No pre-dated, pre-printed CoAs.
Comprehensive Contaminant Panel
Heavy metal testing by Atomic Absorption Spectroscopy (AAS); comprehensive microbiological panel, and strict moisture/ash control matched to your application sector's safety standards.
Raw Material Traceability
Every batch is traceable to its raw herb source: growing region, cultivation or wild-harvest classification, collection season, identity test result, and incoming QC inspection record. For custom products we can source from named cultivation bases and provide farm-level traceability documentation on request.
"We will not issue a CoA that we are not prepared to stand behind."
All quality claims for custom products are handled directly by our QA manager — not routed through sales. If a compliance question arises after delivery, you receive a formal written response with root-cause analysis within 5 business days. We have never refused a quality investigation request from a customer.
Independent third-party testing by your nominated laboratory is welcomed and encouraged. Retained samples are available for third-party retesting at any point within the 24-month window.
- Sample CoA — Astragalus, Drinking Water Grade
- Product Specification Sheet (all 4 grades)
- Heavy Metal & Pesticide Residue Panel
- GMP Facility Certificate
- Raw Herb Origin & Traceability Statement
- Stability Study Summary (24-month)
24-Month Retained Sample & Stability Programme
Every batch across all four grades is enrolled in our 24-month stability programme using dedicated stability test chambers. Real-time and accelerated testing at 6 checkpoints provide formal reports for regulatory dossier submission.
Questions buyers
ask before they commit.
Every question below comes from a real buyer conversation. We answer them here because we would rather address your concerns transparently on this page than have you discover an awkward answer two months into a development project.
GMP&ISO Certified Facility
NMPA-issued GMP certificate, publicly verifiable
University R&D Partnerships
Lanzhou University, Henan Agricultural University, Shanxi Agricultural University
Mutual NDA Available
Signed before any formula details are shared with our team
Export Documentation
Seamless global logistics and compliant documentation for our premium botanical extracts.
What is the minimum order quantity for a custom product?
There is no minimum for the development phases. A lab-scale feasibility sample is typically 20 g – 100 g. A pilot batch is 200–500 kg. For the first commercial batch, minimum quantities vary by extract type and application — discuss your requirement and we will find a workable arrangement. Buyers at the R&D or regulatory submission stage regularly work below standard commercial minimums.
How much does custom development cost?
The initial feasibility assessment (Phase 0) is free of charge.
For Phase 1 (lab-scale development and certified sample), costs depend entirely on the complexity of the project. Minor specification adjustments to our existing botanicals often incur minimal to no development fees (buyer covers shipping). For entirely new extractions or complex multi-herb compounds, a formal development fee is quoted.
Crucially, this development fee is fully credited against your first commercial orderabove a standard volume threshold. Phase 2 (pilot batch) is quoted after Phase 1 completion. We provide afixed-price proposal before any custom phase begins — no open-ended billing.
How do you guarantee the manufacturing date is genuinely current?
Every custom batch is produced against a specific purchase order — we do not maintain pre-manufactured inventory for custom products. The comprehensive batch manufacturing record documents the actual production timeline.
The CoA testing date typically follows the final production date by 3–5 business days (the standard incubation time required for rigorous microbiological clearance). If you have any questions about the manufacturing date of a batch you have received, you can request the original production logs, and we will provide them within 2 business days.
Our GMP-compliant batch records are strictly controlled — they are recorded contemporaneously on the factory floor and undergo dual Quality Assurance review before release, ensuring absolute date integrity and eliminating the possibility of backdated stock.
What if the lab sample doesn't meet my specification?
The purpose of Phase 1 is precisely to determine whether your target specification is achievable before any commercial commitment is made. If our first development attempt does not reach the target, we present you with the analytical data, explain the technical limitation, and propose either a modified target or an alternative approach. You are never obligated to proceed to Phase 2 if you are not satisfied with the Phase 1 outcome. If the specification is technically unreachable, we will tell you clearly at Phase 0 assessment — before you spend a development fee.
Can you source certified organic raw material?
Yes. We have supply agreements with GAP-certified cultivation bases for our major herbs, and access to USDA-NOP and EU-organic certified raw material for a growing list of species. Please specify certified organic material in your brief. We will confirm availability at Phase 0 and include relevant certifications in your documentation package. Organic-sourced raw material carries a premium, disclosed at quotation.
Can I visit your facility or conduct a virtual audit?
Absolutely. Factory audits are welcomed and encouraged. We can arrange a facility tour and technical meeting in Henan at any point in the development process. For buyers who cannot travel, we offer a documented virtual audit: recorded facility walkthrough with live Q&A, full QMS document pack, and batch-level traceability demonstration. Most of our European and North American customers complete their first audit virtually and conduct in-person visits on subsequent order cycles.
Do you offer private labelling and white-label packaging?
Yes. All custom products can be delivered under private label. We package in drums, bags, or smaller retail SKUs with your brand name and label design. Our name does not appear on the outer packaging unless you specifically request it. All private-label arrangements are covered by the project NDA. We do not reference your brand or product in our own marketing materials without written permission.
What happens to the retained sample after 24 months?
We notify you by email at the 23-month mark, giving you one month to request testing or physical return of the retained sample before disposal per our SOP. For products undergoing active regulatory registration, we will extend the retention period beyond 24 months on request. The final 24-month stability test result is issued as a formal written report and added to your product documentation file.
Tell us what
you need.
We'll take it from there.
Whether you need an in-stock grade, a custom specification, regulatory documentation, or a facility audit — the right person on our team will respond within one business day.
Request a Free 20-100g Sample
Any product. Any grade. Worldwide express dispatch within 48 hours.
Request a Bulk Pricing Quote
Get transparent, tier-based pricing for standard extracts or custom formulations. Includes CIF/FOB freight estimates. Fast response within 12 hours.
Submit a Custom Formulation Brief
New botanical, new grade, or compound formula — free feasibility assessment within 48 hours.
Schedule a Factory Audit or Technical Call
Speak directly with our commercial directors or arrange a virtual tour of our Lushi extraction facility. No scripts, just solutions.
All enquiries confidential · NDA available on request · No unsolicited follow-up · One business day response guaranteed
Send us a message
We reply within 1 business day with pricing, lead time, and sample tracking number.