A supplement manufacturer built for European brands.
EUPHM supplies brand owners and distributors in Europe, North America, the Middle East and Asia. Production runs at the Huadu plant of Zhongci Health Products Technology Development Co., Ltd.; EUPHM holds the specification, the documentation and the order. We do not operate a consumer brand of our own.
Contract manufacturing only.
EUPHM (European United Pharmaceuticals) is a supplement contract manufacturer: we develop formulas and produce capsules, tablets, softgels, gummies, powders and liquids. Manufacturing runs at the Huadu plant of Zhongci Health Products Technology Development Co., Ltd.; commercial, regulatory and export work is handled from the Hong Kong office.
- Plant in Huadu, Guangzhou
- Twelve dosage forms
- 1,000 units MOQ per SKU
- Export documents with every batch
Every number below is one we can put a document behind.
- 11
- Years manufacturing
- 10,000
- m² GMP plant
- 35+
- Production lines, group-wide
- 7
- Certifications on file
From one solid-dosage line to twelve dosage forms.
Capacity was added dosage form by dosage form rather than through acquisition. The milestones below mark the capability turns; the full history is available during due diligence.
- 2015
Company founded in Guangzhou
The group's first trading and R&D company is established in Guangzhou, supplying health products to domestic and export customers.
- 2019
National High-Tech Enterprise
Recognised as a National High-Tech Enterprise, with more than ten invention patents and dozens of utility model patents filed.
- 2020s
10,000 m² cleanroom plant
A 10,000 m² visual GMP production base with a class 100,000 cleanroom enters operation in Huadu, Guangzhou.
- 2024
Seven certifications on file
GMP, ISO 9001, ISO 22000, HACCP, NSF/ANSI 455-2, Halal and FDA facility registration held for the Guangzhou site.
- 2025
Hong Kong origin programme
Processing and documentation in Hong Kong: Certificate of Origin or Certificate of Origin Processing, Free Sale Certificate and Food Inspection Certificate; approximately 20 days cross-border.
- Today
Audit-ready operations
Batch record, CoA and retained sample kept for every run; 35+ production lines across the operator’s sites and capacity for 1 billion tablets a year.
Scope of work and exclusions.
The work we accept and the work we decline are listed here and confirmed item by item before quotation.
- OEM production to client formulas
- ODM development by our formulation team
- Private-label packing and export documents
- 1,000-unit MOQ (5,000 for selected formats)
- GMP, ISO 9001, ISO 22000 and HACCP systems
- FDA facility registration and market documents
- Hong Kong origin and finishing, where required
- Operate a supplement brand of our own
- Copy a competitor's protected formula
- Manufacture pharmaceuticals, devices or injectables
- Claim a certification we cannot document
- Broker production without a named, auditable plant
- Promise regulatory approval for an unconfirmed market
Four operating principles.
These apply to every project, regardless of order size.
- 01
Realistic commitments
Lead times are quoted at levels we can hold. Raw-material shortages are reported when they occur, not in the final week.
- 02
One project owner
Each project has a named contact rather than a shared inbox; the same person owns the formula from sample to shipment.
- 03
Documentation first
COA, MSDS, specification sheet and stability data are included as standard, not sold as extras.
- 04
Compliance-aware
Dosage and claim conflicts for the target market are flagged before artwork is commissioned.
Four named owners per project.
Clients do not re-brief a new contact each week; the same four roles carry the project from quotation to shipment.
- 01
Formulation chemist
Converts the brief into a manufacturable formula and owns the bench prototype and stability work.
- 02
QA and regulatory lead
Releases each batch and verifies certificates, labels and market documentation.
- 03
Project account manager
Single point of contact for quotation, samples, artwork and lead time.
- 04
Production and logistics
Scheduling, materials, packing and export documents, so the lot stays traceable after it leaves.
The Huadu plant: twelve dosage forms, one quality system.
A 10,000 m² plant with a class 100,000 cleanroom and five automated solid-dosage lines (35+ across the operator’s sites). Each dosage form runs in its own hall with dedicated air handling, and the on-site quality laboratory releases every batch. Bulk production, packing and export documentation are handled at the same site.
- GMP halls, dedicated air handling
- On-site quality laboratory
- Batch record, CoA and retained sample
- Hong Kong finishing and origin papers
Who you contract with, and who makes it.
Two companies, two roles. A supplier audit starts with the certificate, and the certificate carries the manufacturer's name — so it is set out here rather than left to be discovered.
- Commercial entity
- European United PharmaceuticalsHong KongQuotations, specifications, order handling and export documents.Room A2, 5/F, Cheung Lung Industrial Building, 10 Cheung Yee Street, Lai Chi Kok, Hong Kong
- Manufacturing entity
- Zhongci Health Products Technology Development Co., Ltd.Huadu District, GuangzhouProduction, batch records and certificates of analysis.
- Certificate holder
- GMP, ISO 9001, ISO 22000, HACCP, NSF/ANSI 455-2 and Halal certificates, and the FDA facility registration, are issued to Zhongci Health Products Technology Development Co., Ltd. for the Huadu site. Copies, issuing bodies and validity dates are provided before an order is placed.
Seven certifications and registrations, held for the Huadu plant.
GMP, ISO 9001, ISO 22000, HACCP, NSF/ANSI 455-2, Halal and FDA facility registration, all issued to Zhongci Health Products Technology Development Co., Ltd. for the Huadu site. Full copies, issuing bodies and validity dates are available on request.
Have a product in mind?
Send us the brief and we will come back with a formulation direction, indicative price and a realistic lead time — usually within one working day.