Sourcing Guides

The detail you need before the enquiry.

Written by our R&D and compliance team for importers — the questions they actually answer on the first call. Ten guides and one question board, maintained by the eight chemists and the compliance staff at our ISO 22716 GMP factory in Heyuan, Guangdong.

These guides answer the questions importers actually ask on the first call — how minimum order really works, how to read a safety data sheet, and what compliance costs per destination market.

Nothing here is a price, a lead time or a specification for your order; those are confirmed against the order itself. Ask for a quotation and a named contact replies within one business hour.

Four things buyers need to know

Every guide is written to be useful on its own, whether or not you ever order from us.

Sourcing Guides

For the buyer who has never imported before.

  • What MOQ means in pet product sourcing
  • How to import pet products from China
  • How to evaluate a pet care manufacturer
  • How to read a pet product MSDS
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Compliance Library

For the compliance officer who blocks the shipment.

  • EU CPNP: a complete guide for pet brands
  • FDA registration for pet care products
  • APVMA requirements for Australia
  • HS codes for pet care products
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How-to Guides

For the product itself — dosage, method, mistakes.

  • How to use cat litter deodorizing powder
  • How to use pet deodorizing spray
  • How to use waterless pet shampoo
  • How to introduce a new shampoo to a cat
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Pet Care Notes

For the problems buyers actually search for.

  • Why does my cat's litter box smell
  • Is it safe to use bleach near cats
  • How often should you bathe a dog
  • Natural vs chemical flea treatments
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Per-market compliance detail

What each destination actually requires, and which of those steps are ours.

US

United States

  • FDA establishment registration — held, and verifiable on request
  • MoCRA-aligned cosmetic GMP records retained per batch
  • MoCRA facility registration and product listing responsibilities are allocated in writing before the first sample
  • State-level requirements vary and are quoted per destination state
EU

European Union

  • CPNP notification dossier prepared and submitted on your behalf
  • Responsible Person coordination inside the EU — you must appoint one, we prepare the dossier
  • REACH and BPR documentation assembled from the ingredient list we hold
  • Bilingual EN / 中文 label artwork, with the responsible-person address block
AU

Australia & New Zealand

  • APVMA registration support for products in scope
  • NICCAS / AICIS ingredient disclosure assembled from our formula records
  • ARTG listing coordination where the product is a therapeutic good
  • Full English dossier — no translation step for AU/NZ clearance

A market not listed here is not a refusal — it is an unquoted one. Send the destination and the product type and we will tell you in writing what we can cover before you commit to anything.

Have a question we have not written up?

Send it. If it is worth asking, it is worth publishing — and we will send you the answer directly in the meantime.

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What buyers are asking right now

The three most recent questions, newest first. A new one pushes the oldest out of sight — and the answer gets written into a guide, so the next buyer finds it without asking.

  • EUAnswered in the guide

    Do I need a CPNP notification before I can sell in the EU — and who files it?

    EU compliance detail
  • USAnswered in the guide

    Who handles customs clearance on the US side — you, or my own broker?

    US compliance detail
  • AUAnswered in the guide

    Is the product already registered with APVMA, or do I have to do that myself?

    AU & NZ compliance detail

0/280 — sent to our sales team on WhatsApp, and shown at the top of the board.