Product formula, product packaging design, product filling volume, etc. can all be customized by customers privately.
Accept the formula provided by the customer and then have it produced by our factory.
If the customer wants a product with a certain function, our researchers will formulate the product formula, and then our factory will carry out the production.
If the customer has their own design style, they can hand over the design documents to the salesperson, and we will arrange for a domestic packaging company to print them. If the client does not have a design team, our company can provide design services.
Formulation, taste, packaging, brand design, OEM, etc.
The customer informs the sales manager of their requirements, and the sales manager will coordinate with the company's order-following staff to handle the entire process of the order.
You have a formula. You need a GMP-certified factory to produce it at volume, with consistent quality and full documentation.
We take your formulation specification and produce it exactly — your active ingredients, your excipients, your concentrations. Our role is precision manufacturing and quality assurance. You retain full IP ownership of your formula.
What you bring: Product formula, target market regulatory requirements, packaging specification.
What we deliver: Finished product to spec, Certificate of Analysis per batch, GMP manufacturing documentation, export paperwork.
You know what you want the product to do. You don't have a formula yet.
Our R&D team formulates the product from scratch based on your functional brief — target species, indication, active ingredient class, dosage form, and any specific performance requirements. Once the formulation is validated and approved by you, production begins under your brand.
What you bring: Product brief (target species, indication, desired format — tablet, spray, spot-on, chew, etc.), brand identity, target markets.
What we deliver: Custom formulation, pilot batch for approval, full-scale production, packaging, and regulatory documentation package.
The fastest route to market. Choose from our existing validated product range, apply your brand identity, and launch.
No formulation development time. No pilot batch approval cycle. Our existing formulations have established stability data, efficacy data, and in many cases existing regulatory registrations in multiple markets. You get proven products under your name, fast.
What you bring: Brand name, logo, label artwork (or we design it for you), target market, order quantity.
What we deliver: Finished labeled product, CoA, and all documentation needed for import clearance in your market.
| Service Element | OEM | ODM | Private Label |
|---|---|---|---|
| Use Your Existing Formula | ✓ | — | — |
| Custom Formula Development | — | ✓ | — |
| Ready-to-Use Validated Formula | — | — | ✓ |
| Custom Brand & Label | ✓ | ✓ | ✓ |
| Custom Packaging Format | ✓ | ✓ | ✓ |
| Packaging Design Service | ✓ | ✓ | ✓ |
| Regulatory Dossier Support | ✓ | ✓ | ✓ |
| Certificate of Analysis (COA) for Each Batch | ✓ | ✓ | ✓ |
| Stability Data Provision | ✓ | ✓ | ✓ |
| Acceptance of Third-Party Audits | ✓ | ✓ | ✓ |
| Sample Batch Before Mass Production | ✓ | ✓ | ✓ |
Our manufacturing capability covers the full companion animal health spectrum. All categories below are available for custom production.
Veterinary Pharmaceuticals (Prescription & OTC)
Antiparasitics: spot-on solutions, oral tablets, injectable formulations (fleas, ticks, heartworm, intestinal worms, ear mites)
Antifungals: topical sprays, tablets, shampoos (dermatophytosis, ringworm, yeast infections)
Antibiotics / Respiratory: oral and injectable formulations
Analgesics / Anti-inflammatories: NSAID class, pain management
Chronic disease management: cardiac, diabetes-adjacent, endocrine support
Nutritional & Health Care Products
Joint support: glucosamine, chondroitin, omega formulations
Liver support: hepatoprotective formulations
Immune & allergy support
Coat & skin supplements
Digestive / probiotic products
Urinary / kidney support
Ear, eye, and oral hygiene products
Heart & circulatory support
Dosage Forms Available
Tablets · Chewable tablets · Soft chews · Capsules · Topical spot-on pipettes · Sprays · Shampoos · Powders · Oral liquids · Injectables (select formulations) · Gels · Ointments
Every element of your product can be specified. Common customization requests we handle:
Formulation: Active ingredient selection and concentration, excipient profile, flavor (for palatability in oral products — chicken, beef, bacon, cheese), texture (chew firmness, tablet hardness), color.
Packaging: Bottle size and material (HDPE, PET, glass), closure type (spray pump, dropper, flip cap, twist-off pipette), blister format, foil sachet, box dimensions and board weight, insert / leaflet design and language.
Labeling: Brand name, logo, product name, claims language adapted to your target market's regulatory framework, barcode (EAN, UPC, or local standard), batch number and expiry format per market requirement.
Language & Market Adaptation: Labels produced in any language. Claims language reviewed against target market regulatory requirements (EU, UK, US, AU, Southeast Asia, Middle East, LATAM) to ensure compliance before print.
Step 1 — Demand Communication (Day 1–3)
Submit your product brief to our sales team via the inquiry form or directly by email/WhatsApp. We respond within 24 hours with a feasibility confirmation and preliminary quotation. A dedicated project manager is assigned to your account from this point.
Step 2 — Sample Development (Day 4–21)
For ODM projects: our R&D team formulates to your brief and produces a pilot batch. For OEM: we validate your formula against our production parameters. For private label: we prepare a labeled sample from existing validated stock. Samples shipped to you for approval.
Step 3 — Sample Approval & Order Confirmation (Day 22–30)
You review the sample. Feedback and adjustments if needed — typically 1–2 revision rounds. Once sample is approved, you confirm the bulk order with a 30% deposit.
Step 4 — Factory Production (Day 31–65)
Full-scale production begins. Your project manager sends weekly photo and progress updates from the production floor. In-process QC checks at each production stage. Pre-shipment QC inspection report prepared.
Step 5 — Product Delivery (Day 66–75+)
Final QC sign-off. Complete documentation package prepared: Certificate of Analysis, GMP certificate, MSDS, packing list, commercial invoice, and any market-specific certificates requested. Goods shipped FOB Tianjin/Shanghai or CIF to your port.
Timeline above is indicative for a standard ODM project. OEM and private label timelines are shorter. Complex formulations or new dosage forms may require additional development time — your project manager will advise at briefing stage.
Buyers in regulated markets require more than a price list. Here is what we provide before you place an order.
GMP Certification — Our facility operates to Good Manufacturing Practice standards for veterinary pharmaceutical production. GMP certificate available upon request.
Quality Management — ISO 9001 quality management system. In-process QC at formulation, filling, labeling, and packing stages. Finished product retained samples held per regulatory requirements.
Regulatory Documentation Package — Every batch ships with: Certificate of Analysis, MSDS, product specification sheet. On request: stability data summary, efficacy study references, ingredient safety data.
Third-Party Inspections — We welcome pre-order and in-production facility audits by SGS, Bureau Veritas, TÜV, or buyer-nominated agencies. Audit scheduling coordinated through your project manager.
Export Track Record — Products shipped to 30+ countries across Europe, Southeast Asia, Middle East, Latin America, and Oceania. Familiarity with import documentation requirements for major markets.
Veterinary pharmaceutical distributors building own-label product ranges to improve margin and brand equity alongside their principal-brand portfolio.
Pet health importers entering new product categories — adding antiparasitic, antifungal, or nutritional supplement SKUs to an existing import book without building in-house formulation capability.
E-commerce pet health brands launching direct-to-consumer ranges that require manufacturer-grade documentation for platform compliance (Amazon, Chewy, and equivalents in EU/UK markets).
Veterinary clinic chains developing house-brand products for in-clinic dispensing — particularly nutritional supplements and preventive care products where regulatory barriers are lower.
Retail pet health brands sourcing private label products at competitive cost with consistent quality across repeat orders.
International trading companies consolidating veterinary product sourcing from a single GMP-certified manufacturer to simplify compliance management.
If you don't have an in-house design team, we do.
Our packaging design service covers primary label, secondary box, insert/leaflet, and display unit design. We work from your brand guidelines or build a brand identity from scratch if needed.
Design output includes: print-ready artwork files (AI/PDF), label proofs for approval before production, language adaptation for multilingual markets, and barcode/batch format integration per your market's requirements.
Design turnaround: 5–7 business days for initial concepts. Typically 2–3 revision rounds before final approval.
What is the minimum order quantity for OEM/ODM production?
MOQ varies by product category and dosage form. Tablets and chewables typically have lower MOQs than complex liquid formulations. Contact us with your specific product brief for a project-specific MOQ and price breakdown.
Can I supply my own packaging materials?
Yes. If you have preferred packaging suppliers or want to use existing stock packaging, we can accommodate this — subject to compatibility review with our filling lines.
Do you sign NDAs before sharing formulation details?
Yes. We routinely sign mutual NDAs before any formulation exchange or proprietary brief discussion. Your IP is protected from the first conversation.
How long does ODM formula development take?
Typically 2–4 weeks for standard formulations (tablets, sprays, spot-ons). Novel formulations or new dosage forms may take 6–8 weeks. Your project manager will give a specific timeline at the briefing stage.
Can you produce products for both dogs and cats from the same facility?
Yes. We manufacture products for dogs, cats, small animals, and in some categories livestock. Cross-contamination controls between species-specific and active ingredient-specific production runs are in place per GMP requirements.
What happens if a batch fails QC?
Failed batches are rejected and not shipped. We conduct a root cause analysis, implement corrective action, and re-produce at no additional charge for manufacturing defects. Your project manager communicates transparently throughout.
Can you handle ongoing repeat orders reliably?
Yes. We maintain approved supplier status with several large international distributors who place quarterly and annual repeat orders. Batch records and retained samples are held per GMP requirements, supporting consistent reorder quality.
