

Supplement manufacturing and project coordination for growing health brands
From benefit definition, formula development, regulatory compliance, pilot sampling and packaging design to scaled production, global export documents and delivery.
Origins
Dosage forms
Certifications
48h
Initial project response
3
Documented production regions
$2,000
Sample development fee, credited to bulk orders
1 team
Formula, packaging, documents and production coordination
Core capabilities
Built for brands that need to test, iterate and scale
We combine low-MOQ manufacturing, new nutrition delivery technology, formula development and compliance support into one managed supply-chain path.
Fast initial project review
Turn a product brief into an initial manufacturing direction covering formula status, dosage form, packaging, documents and the next decisions needed for a usable quote.
Low MOQ, sampling and trial production
Coordinate project-specific sampling and trial production. The USD 2,000 sample development fee is credited to a subsequent bulk order; production MOQ is confirmed after the formula, format and packaging are reviewed.
Documented multi-location production resources
Coordinate suitable resources in Shanghai, Hong Kong and Singapore, with one project team managing formula review, packaging, applicable documents and delivery planning.
New nutrition delivery technologies
Coordinate cocrystal, microencapsulation, nano and liposomal technology paths to improve stability, taste and bioavailability.
Herbal and compound formula capability
Combine Asian botanical extracts with mainstream Western nutrition ingredients to build differentiated formulas for target audiences.
International project coordination
Use practical experience supporting established supplement brands across different dosage forms and production requirements to reduce communication gaps during development and scale-up.
Our factories and partner lines
A documented manufacturing network across three production regions
We coordinate production through long-term factory partners and hold ownership interests in selected partner facilities. The applicable production route is confirmed for each project.
Entity note: Hangzhou Hengyang Technology Co., Ltd. manages commercial communication and the project. When the Shanghai route is selected, Shanghai Yaoshenfeng Biotechnology Co., Ltd. is the manufacturing entity for formula review, production and applicable documents.
A clear manufacturing route
The applicable manufacturing entity, production location and document path are identified for the project instead of being hidden behind a generic supplier claim.
Direct access to the formulation team
Questions about ingredients, stability or taste go straight to the people running the lines — answers in days, not weeks.
One accountable project team
Formula review, sampling, packaging, applicable documents, production follow-up and delivery planning are coordinated through one team.
Invested manufacturing partnerShanghai, China
Shanghai Yaoshenfeng Biotechnology
Jinshan District, Shanghai
- An invested Shanghai manufacturing partner supporting supplement production, product development, documentation and customized packaging.
- Tablets, softgels, vegetarian softgels, hard capsules, gelatin and vegetarian capsules, powder and liquid formats.
- Private label and packing available on site.
- Documented NSF GMP for Dietary Supplements, HACCP and GRMA qualification references are available for review.
Invested manufacturing partnerHong Kong
BoSang Yotta Solutions Pharmaceutical Factory
Kwai Tsing District, Hong Kong — manufacturing, packing and document support
- An invested Hong Kong manufacturing partner for capsules, softgels, powders, tablets, health foods, confectionery products and solid drinks.
- The facility supports formulation, manufacturing, packing and documentation for multiple supplement dosage forms.
- The natural choice when a buyer needs Hong Kong origin, Hong Kong warehouse delivery, cross-border ecommerce dispatch or flexible trade documentation.
- FEHD food factory licence, U.S. FDA facility registration, FSSC 22000, ISO 22000, HACCP, GMP and SGS on-site audit references.
Additional documented production partners
Singapore
Documented production partnerDocumented manufacturing partners — Singapore
Kim Sin Medicine Manufactory and Harmony Pharma Lab provide documented Singapore production resources that may be mobilized when the project and product category fit.
Certificates and documents are provided where applicable, depending on facility and destination market. On-site and video factory audits are welcome.
Factory credentials
Certificates across our factory network
Representative certificates available for public display. Full certificate files are provided per order — on-site and video audits welcome.


HACCP Certificate

HACCP Certificate · Page 2

GRMA AuditSphere Certificate

GRMA AuditSphere Certificate · Page 2

FSSC 22000 Certificate

SGS GMP Certificate

U.S. FDA Facility Registration

GMP Certificate (Singapore HSA)
Origin comparison
Which production origin fits your order
One project team coordinates documented resources in Shanghai, Hong Kong and Singapore. The final route depends on formula, format, packaging, documents and delivery requirements.
| Origin | Type | Best for | Typical MOQ | Typical lead time | Documents |
|---|---|---|---|---|---|
| Shanghai, China | Long-term partner facility | Broad dosage-form capability, packaging coordination and scalable production | Confirmed per formula, process and packaging | Confirmed after feasibility and material review | NSF GMP, HACCP, GRMA and project-specific product/export documents where applicable |
| Hong Kong | Long-term partner facility | Hong Kong production, packing and document support across multiple dosage forms | Confirmed per formula, process and packaging | Confirmed after feasibility and material review | FEHD licence, FDA registration, FSSC 22000, HACCP, COA, COO |
| Singapore | Documented production partners | Projects suited to the documented capabilities of Singapore partner resources | Confirmed per project | Confirmed per project | HSA / PIC/S GMP references and other documents as applicable to the selected entity |
MOQ and lead times are typical reference values and vary by dosage form and formula status; the quotation is definitive.
Hero products and innovation
Launch-ready directions for differentiated supplement SKUs
Use proven consumer formats and formula stories to move faster from product idea to sample discussion.

Sugar-Free Chewable Softgel (Plant-Based)
Sugar-Free Chewable Softgel
A sugar-free chewable alternative to high-sugar gummies — an advanced plant-based gel shell delivers the gummy experience without the sugar load.
- Replaces high-sugar gummies: chewable, tasty, and sugar-free.
- Chew directly without water — ideal for children, seniors and capsule-averse consumers.
- 100% plant-based shell supports vegan and religion-friendly positioning.




Liposomal Liquid Technology
Nano-Liposomal Liquid
A liquid delivery route for selected water-insoluble ingredients. Formula feasibility, dispersion, stability and any performance evidence are reviewed ingredient by ingredient.
- Emulsifies water-insoluble actives such as CoQ10 and curcumin into stable liquids.
- Reference-test results are ingredient- and method-dependent and are not presented as a universal product claim.
- Opens ready-to-drink shots, drops and spoonable formats beyond capsules.

Delivery Technology Portfolio
Delivery Technologies
Several delivery paths can be assessed against the active ingredient, stability target and desired consumer experience.
- Cocrystal and microencapsulation improve stability and mask taste.
- Hydrogel and nano-emulsion directions can be evaluated where the formula and process support them.
- Every delivery-technology claim is tied to the selected material, formula and available evidence.
AI-Assisted Packaging Development
Quickly explores packaging visual directions before formal design, artwork production and regulatory label review, reducing early communication and trial costs.
- Rapidly explore multiple visual directions around brand positioning, ingredients and target users.
- Apply directions to bottle, box and pouch SKUs for practical comparison.
- Move selected directions into professional design, artwork and regulatory label review.

Liquid CoQ10 (liposomal)
A liquid delivery direction for selected fat-soluble ingredients. Feasibility, dispersion, stability and any performance comparison must be confirmed for the specific ingredient and formula.

Live probiotic products
Capsule and powder options for live probiotic formulas, with strain, target count, manufacturing loss, moisture protection, packaging and shelf-life controls reviewed for each project.
Managed launch path
From idea to a controlled production handover
A milestone-based path for formula review, sampling, packaging, production, documents and delivery. Timing is confirmed for the actual project.
Stage 1
Direction alignment
Confirm target benefit, audience, dosage form, market and budget.
Stage 2
Fast quotation
Complete preliminary cost estimation for formula, packaging and production.
Stage 3
Intent contract
Confirm development scope, milestones, fees and delivery standards.
Stage 4
Sampling and packaging
Run formula sampling, taste adjustment and packaging design in parallel.
Stage 5
Formal production
Complete raw material purchasing, manufacturing, quality checks and finished packaging.
Stage 6
International logistics
Arrange export documents, transportation and destination delivery.
Compliance & documentation
The paperwork overseas buyers expect
We help coordinate the documents your market and channel require, with honest, conditional wording.
Availability depends on the factory and destination market. We do not guarantee that every document is available for every order.

Use cases
Built for how supplement brands actually launch
Wherever you are in your journey, we plug into the gaps and manage the rest.
Amazon seller launching first supplement SKU
DTC brand seeking an additional Asian manufacturing route
Existing brand expanding into new dosage forms
Distributor needing origin and export documents
Overseas exhibitions
Eight years of international exhibition presence
Our booths at international supplement exhibitions keep us close to what overseas buyers actually ask for — dosage forms, packaging expectations, pricing and launch timelines.



The Supplement Sourcing and Compliance Checklist
Everything overseas brands need before placing a first manufacturing order — labeling, documents, MOQ and formula selection in one practical PDF.
- Country-by-country labeling requirements
- Required export documents checklist
- MOQ & cost planning worksheet
- Formula and dosage-form selection guide
FAQ
Questions overseas brands ask us
Short, factual answers. For anything specific to your order, send us a brief.