Exporting Food and Cosmetics to China: Four Steps
Check the HS code, register the trademark, get a Cypher ID under GACC Decrees 248 and 249, and produce the Chinese counter-label. In that order.


Product name, HS code and technical data, enough for us to scope the route.
Your part
A specialist confirms the regulations that apply and the document type your product needs.
Our part
You send the supporting documents; we sign a contract with fixed scope and timeline.
Both sides
Laboratory testing, factory inspection and customs clearance, coordinated by us.
Our partIssued, registered, and delivered. We close the project.
Your partThere is no single food certification accepted everywhere. What travels is the system: a documented HACCP plan underpins nearly every national regime and every buyer scheme. On top of it sit two things that are easy to confuse. GFSI-benchmarked certification such as BRCGS or FSSC 22000 is what a buyer writes into the supply contract. The legal requirement of the destination is something else: registration of the facility, an EAC declaration or state registration in the EAEU, a health certificate, and labelling in the local language.
A documented HACCP plan is what nearly every regime assumes: Article 5 of Regulation (EC) 852/2004 in the EU, Article 10 of TR CU 021/2011 in the EAEU, 21 CFR Part 117 in the US.
Audits fail on monitoring records, so measure the limits and evidence corrective actions.
BRCGS, FSSC 22000, IFS or SQF is what a retailer writes into the supply contract. No government asks for it, and a fully registered plant can still lose the buyer without one.
A BRCGS certificate does not replace the establishment listing a destination requires.
Set by the destination: FDA facility registration and prior notice, EU establishment listing under Regulation (EC) 853/2004, an EAC declaration or SGR in the EAEU, GACC Decree 248 registration for China.
Start facility registration months before shipment, because finished goods do not speed it up.
Food export programmes slip in the same places. Facility registration was started last, after production for the market was scheduled, and GACC registration under Decree 248 or an EU establishment listing takes months that a finished consignment cannot shorten. A BRCGS certificate was bought for a destination that wanted a listing. Or the HACCP plan exists, while its monitoring records show critical limits nobody measured and corrective actions nobody evidenced.
Registration regimes such as GACC Decree 248 attach to the establishment and the product category. The EU listing for products of animal origin is made on the nomination of your own country's competent authority, and the exporter cannot file it directly. Your HACCP monitoring records are the site's history, and an auditor reads them first. A halal certificate works only where the destination recognises the body that issued it.
What we handle
Everything here is something to find before the project starts. The first reply says which of it can go into the file as it is.
One specialist owns your file from the first email to the registered certificate. Every one of them has recorded a briefing on their field.
Each stage is a service of its own, with a page that says what it produces and what it needs from you.
The cheapest stage decides the cost of every stage after it. What a route assessment names, and the four decisions it locks down.
Read the pageAccreditation is per standard and per laboratory, never general. How to choose one the destination accepts, and test once for several markets.
Read the pageThe file is the certificate’s foundation and it is the manufacturer’s to produce. What it has to contain, and what cannot be written retrospectively.
Read the pageAudits turn a schedule from weeks into months and cannot be compressed. What auditors check, and how to be ready for the first visit.
Read the pageFour major markets refuse to certify a foreign manufacturer directly. What the appointment obliges, and why a distributor is the wrong holder.
Read the pageA correct certificate and a wrong label still stops at the border. What each market demands on the artwork, and when to check it.
Read the pageExporters routinely conflate two obligations. The first is regulatory: whatever the destination government requires before the goods clear customs. In the United States that is FDA facility registration and prior notice, with preventive controls under 21 CFR Part 117. In the European Union it is the hygiene rules of Regulation (EC) 852/2004, third-country establishment listing under Regulation (EC) 853/2004 for products of animal origin, and labelling under Regulation (EU) 1169/2011. The second is commercial: whatever the retailer or importer writes into the supply agreement, which for a large retailer is a GFSI-benchmarked scheme.
A plant can hold a flawless BRCGS certificate and still be unable to ship, because the destination requires an establishment listing it does not have. The reverse also happens: fully registered, legally able to export, and refused by the buyer for lacking a certificate no government asked for.
In the Eurasian Economic Union food is regulated by TR CU 021/2011 on food safety, which applies to every product and every process. Most food is placed on the market on an EAC declaration of conformity registered in the unified register, and Article 10 of the same regulation obliges the producer to run HACCP-based procedures. Specialised food, novel food and food for infants take state registration (SGR) from a member state's health authority instead of a declaration, and that certificate has to exist before the first consignment is placed on the market.
Two more regulations sit on almost every file. TR CU 022/2011 sets the label: Russian-language name, composition, allergens, dates and the EAC mark. TR CU 029/2012 covers additives, flavourings and processing aids, and a colourant or sweetener missing from its permitted lists blocks the declaration. Sector regulations add a layer for juices (TR CU 023/2011), fats and oils (TR CU 024/2011), milk (TR CU 033/2013), meat (TR CU 034/2013) and fish (TR EAEU 040/2016).
Hazard Analysis and Critical Control Points is a method, and it is the foundation almost every other requirement builds on. GFSI schemes assume it. The EU requires it through Article 5 of Regulation (EC) 852/2004, the EAEU through Article 10 of TR CU 021/2011, and the United States through the preventive-controls rule in 21 CFR Part 117, which is HACCP with a wider hazard list.
Where HACCP plans fail audit is rarely the hazard analysis itself. It is the monitoring records: critical limits set but never measured, corrective actions described but not evidenced, verification scheduled and not performed. An auditor reads the records first.
Halal is a separate scheme with its own audit and its own recognition rules, and the destination decides whether a certificate works, whoever issued it. It is covered in full on halal certification, including which authority accredits whom and the Indonesian deadline.
Several markets require the producing establishment to be registered before any consignment moves. China runs overseas producer registration under GACC Decree 248, in force since 1 January 2022, through the CIFER system, and an unregistered facility cannot export the listed categories at all. Brazil requires product registration or notification through ANVISA depending on category. The EU lists third-country establishments for products of animal origin on the nomination of the exporting country's competent authority, so the exporter cannot file that one directly.
These are lead-time items measured in months, and they are the most common reason a food export programme slips. They cannot be started once the goods are made, because the registration attaches to the facility and the product; a finished consignment does not speed it up.
| Market | Legal requirement | What buyers additionally expect |
|---|---|---|
| Gulf states | Halal certificate from a recognised body; conformity scheme registration; Arabic labelling | HACCP or a GFSI scheme |
| European Union | Establishment listing for products of animal origin (Regulation (EC) 853/2004); health certificate; labelling under Regulation (EU) 1169/2011 | BRCGS, IFS or FSSC 22000 |
| EAEU | EAC declaration under TR CU 021/2011, or SGR for specialised, novel and infant food; labelling under TR CU 022/2011; additives under TR CU 029/2012 | HACCP |
| China | GACC facility registration under Decree 248; product-specific requirements; Chinese labelling | HACCP, often a GFSI scheme |
| Brazil | ANVISA registration or notification by category; Portuguese labelling | HACCP |
| United States | FDA facility registration; prior notice; preventive controls under 21 CFR Part 117 | SQF or BRCGS |
Requirements vary sharply by product category within each market; a shelf-stable ambient product and a chilled product of animal origin are different regimes. Treat this as the shape of the problem and check the specification for your category.
A HACCP system is mandatory or effectively mandatory almost everywhere; a HACCP certificate is not. The EU under Regulation (EC) 852/2004, the EAEU under TR CU 021/2011 and the United States under 21 CFR Part 117 all require you to operate the system and evidence it at inspection, and none of them asks for a third-party certificate. Buyers are a different matter and frequently ask for one, either HACCP or a GFSI-benchmarked scheme that includes it.
HACCP is the underlying hazard-control method. ISO 22000 is a management system standard that incorporates HACCP but is not itself GFSI-benchmarked. BRCGS, FSSC 22000, IFS and SQF are GFSI-benchmarked schemes, which is what most large retailers accept. FSSC 22000 is the common bridge for a plant already certified to ISO 22000, since it builds on that standard and adds the prerequisite programmes GFSI expects.
No, and assuming so is a common error. Each destination recognises a specific list of certification bodies, and those lists differ and are revised. A certificate from a body recognised in one Gulf state may not be accepted by its neighbour. Confirm which bodies the destination currently recognises before commissioning the audit.
Before production for the target market is scheduled, and ideally before the commercial agreement is signed. Registration regimes such as GACC Decree 248 in China attach to the establishment and the product category, take months, and cannot be accelerated by having goods ready. It is the item most likely to delay a launch and the one most often started last.
Check the HS code, register the trademark, get a Cypher ID under GACC Decrees 248 and 249, and produce the Chinese counter-label. In that order.
Which products need it, which certification bodies the GCC actually recognises, and the audit and laboratory stages between application and certificate.
Registering on the GACC platform, the certificates needed before you can, local quarantine testing, Chinese labelling and the eight documents customs asks for.
Send the product name, HS code and technical data. You get back the applicable route, the document list and a timeline, before any commitment.