According to the certification system of the Eurasian Economic Union (EAEU), EAC certification is primarily divided into the following four types, as summarised below based on historical dialogue and search results:
1. EAC Declaration of Conformity (DoC)
Applicable products
Medium- and low-risk products (such as certain electronic devices, building materials, and daily chemical products).
Perfumes, cosmetics, etc. require SGR registration for use.
Certification Characteristics  
Self-declaration by the applicant: The manufacturer or importer is responsible for the product's compliance, and no certification body is required to issue the certificate.  
Validity Period: Single batch (limited to specific contracts) or series production (up to 5 years).  
Document Requirements: Test reports, technical documents, and purchase contracts must be provided (mandatory for single-batch certification).

2. EAC Certificate of Conformity (EAC CoC)  
Applicable Products
High-risk products (e.g., machinery, children's products, pressure vessels, etc.).  
Certification Features  
Third-party institution issuance: Reviewed and issued by an EAEU-accredited certification body.  
Process Requirements:  
Document review + sample testing (at an EAEU-accredited laboratory).  
Factory audit may be required (process duration up to 3–4 months).  
Validity Period: Up to 5 years.

III. State Registration Certificate (SGR)  
Applicable Products  
Health and safety-related products: food, cosmetics, disinfectants, children's products, etc.  
Note: Perfumes/cosmetics must obtain both the EAC Declaration and SGR.  
Certification Features  
Competent Authority: Issued exclusively by Rospotrebnadzor (Russian Federal Service for Supervision of Consumer Rights Protection and Human Welfare).  
Permanent Validity: Once registered, there is no expiration date, but test reports must be updated periodically.
Special Requirements: Some products (e.g., laundry soap) require an additional GOST-R Conformity Declaration.  ,
  
4. Medical Device Registration (MR)  
Applicable Products  
All medical devices (e.g., surgical instruments, diagnostic equipment, implants, etc.).  
Certification Characteristics  
Independent Regulatory Framework: Based on the Eurasian Union's ‘Technical Regulations on the Safety of Medical Devices’ (No. 156).
Mandatory registration: Clinical assessment and technical review must be completed prior to market entry.
No EAC mark: However, registered products may circulate within the five EAEU member states.

Key Comparison Summary
Type    Scope of Applicable Products    Issuing Authority    Validity Period    Special Requirements
EAC Conformity Declaration    Medium-to-low-risk products    Self-declaration by the applicant    ≤5 years    Test reports required
EAC Conformity Certificate    High-risk products    Certification body    ≤5 years    Factory audit (if necessary)
National Registration Certificate (SGR)    Health-related products    Rospotrebnadzor    Permanent validity    Regular testing updates required
Medical Device Registration    Medical devices    Ministry of Health-authorised institution    No fixed term    Clinical assessment and technical review
Notes:

Cosmetics/perfumes require both EAC declaration + SGR;
Single-batch certification requires purchase contracts and invoices.
For more cases, please refer to the original search results:

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