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Electronic conformity documents: how the FGIS register works

A document gets its legal force from the record in the state register, not from a form on security paper. This changes the way of checking: you need to look not at the document but at the record about it.

Just a few years ago, checking a document came down to examining the form: the hologram, the seal, the signature. Today none of this matters — what matters is the record in the state information system.

What the record contains

Fields to compare
01ApplicantWho issued the document and has the right to use it
02ProductName, features, HS codes (TN VED)
03BasisTest reports and the assessment scheme
04StatusValid, suspended, terminated, declared invalid
A mismatch in even one field is a reason not to accept the document.

How to read the statuses

StatusWhat it meansCan the goods be sold
ValidThe document is in force, the term has not expiredYes
SuspendedValidity is temporarily stopped until the causes are eliminatedNo
TerminatedValidity ended on application or by decisionNo
Declared invalidThe document is considered to have had no force from the moment of registrationNo, and a product recall is required
ArchivedThe validity period has expired naturallyFor goods released during the validity period — yes
An important difference Expiry of the term and being declared invalid are different things. In the first case, goods put into circulation in time can be sold until the end of their shelf life. In the second, the document is considered never to have been in force.

What a counterparty sees

The register is open: any buyer, marketplace or customs authority can check a document by its number. This changes the practice of work — it is impossible to hide a problem status, and a discrepancy between the product card and the record in the register is found within a minute.

Order of checking before a deal

Frequent discrepancies

What occurs

  • The register has one modification, the delivery has another
  • The manufacturer in the document does not match the actual factory
  • The HS codes (TN VED) in the record do not cover the imported goods
  • The test report was issued by a laboratory whose accreditation was terminated

How to react

  • Request a document for the required modification
  • Clarify the production site and make changes
  • Issue a document with the correct list of codes
  • Demand retesting in a laboratory that is currently accredited

What to do if the document was suspended after sales had already started is covered in a separate review. How to choose a laboratory so as not to get into this situation is covered here.

What is needed to register a declaration yourself

Registering a declaration is an action of the applicant, and an intermediary is not mandatory for it. The set of requirements is small, but every item is blocking: without any one of them the procedure will not start.

The most frequent delay is the signature. Issuing it takes time, and without it you can neither submit nor sign. If the declaration is needed by the delivery date, the signature is arranged first, not last.

Responsibility is not shared with an intermediary Whoever technically enters the information, the applicant is responsible for its accuracy. The wording “this is how it was prepared for us” does not work: the register carries your name. That is why the text of the declaration is read in full before signing, and not signed once payment is made.

What the buyer’s check of a document looks like

It is useful to look at your document through the eyes of the one who will check it: a retail chain buyer, a platform manager, a customs representative. They all look at the same things.

  1. They find the record by number — if there is none, the conversation goes no further.
  2. They compare the status: valid, suspended, terminated, archived.
  3. They compare the name of the product with what is on the packaging and in the card.
  4. They look at the manufacturer: whether it matches the one stated on the label.
  5. They check whether the document was valid on the date of delivery, not only today.
  6. For the batch scheme — they compare the batch information.
  7. They check the laboratory from the test report: whether the accreditation is valid and whether the scope is the right one.

Each step takes seconds, so counting on “they will not notice” does not pay off. How to read a laboratory card is covered in a separate article.

What to do about an error in a registered declaration

A typo in the name, a wrong HS code (TN VED), an incomplete list of models — these are usually found after registration, when the document has already gone to counterparties.

A practical rule: the earlier an error is found, the cheaper it is. For a declaration under which half a year of deliveries has already been shipped, reissuing leaves open the question of what covered those shipments.

Paper copy and electronic record

A question that still causes disputes at acceptance: is a printout with a seal needed. Legal force comes from the record in the register, not from paper. A printout is a convenient form of presenting the information, nothing more.

Practical consequences follow: a scan without a record in the register confirms nothing; a seal on a printout adds nothing; if the paper and the register differ, the record in the register is correct. If a counterparty insists on an “original with a blue seal”, the simplest thing is to send a link to the register card — it holds the same information at its primary source.

Check your product Describe your product in plain words — the system will show the expected HS code (TN VED), the applicable regulations and the set of documents. Start the check.
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