Registration process

Export registration

Product range

Feed additives, veterinary drugs, etc

Service process

Evaluation of products and documents → signing of registration agreement → material preparation (evaluation, rectification and translation) → submission to relevant departments of the importing country to follow up and modify the documents until they pass the review → mailing of samples → issuance of certificates

Prepare materials (1-7 documents are often used for consulate certification, 8-18 common registration documents, and different registration document requirements in different countries)

1. GMP, ISO, FAMIQS certificates

2. Certificate of free sale

3. Letter of authorization

4. Manufacturing license

5. Product approval document (certificate of registration)

6. Certificate of origin

7. GMO free certification

8. Composition

9. Flow chart and process

10. Analysis method (finished product / raw material)

11. Analysis result (finished product / raw material) (certificate of analysis)

12. Stability experiments and chromatograms

13. SPC(SUMMARY OF PRODUCT CHARACTERISTICS)

14. Package, label and brochures

15. MSDS(Material safety data sheet）

16. Third party laboratory report (inspection report)

17. TDS(TECHNICAL DATA SHEET)

18. Literature (effectiveness study, toxicology study, maximum residue study, safety study)