3. Key facts
Foreign companies must register their products and obtain the registered
license before selling in china.
The license is valid for 5 years.
The responsible authorities are:
The Ministry of Agriculture (MOA)
China National Feed Quality Control Center
China Institute of Veterinary Drugs Control (CIVDC)
*This process is subject to change
4. Registration diagrams for imported feed, feed additives & veterinary drugs
Imported Feed Additives (Two Types) Imported Veterinary Drugs
Type 1: On list of approved feed Type 2: Not on list of approved
and feed additives feed and feed additives
Dossier preparation
Dossier
preparation
Dossier
preparation Preliminary review by
Preliminary review MOA
by MOA
Clinical trials and
Preliminary Feeding test and residue tests
review by MOA safety test
Evaluation
Evaluation
Quality test
Quality test Quality test
License approved License approved
License approved
6. Registration for Type 1 products
TIME
Registration
How we help
Dossier
procedure
Months Hours preparation
1. Dossier
3 300 Organization
preparation
Preliminary
review by MOA
2. Preliminary review
1 Connections
by MOA
50
3. Quality test 3 Experience
Quality test
4. License approved 1 Speed
Total 8 350
Note: ①The" Months" is the time the whole registration will take from the beginning to the License
end. approved
②The "Hours" is the time I will spend on this registration.
7. The approved feed additives
The approved feed additives are composed of 13 categories of feed additives. They are:
Amino acids (23)
Vitamins (32 )
Minerals and their complexes(chelates)
Enzymes (13)
Live Micro-organisms (16)
Non-protein nitrogen (9)
Antioxidants (4 )
Preservatives and Acidity Regulators (30 )
Coloring Agents (7)
Seasonings and Flavoring Agents (4 feed and other human food additives)
Binders, Anti-caking Agents and Stabilizers (32)
Polysaccharides and Oligosaccharides (5 )
Others (14)
*Note: The list is from No.1126 announcement of MOA.
9. Registration for type 2 products
TIME Dossier
Registration
procedure
How we help preparation
Months Hours
1. Dossier
preparation
4 500 Organization Preliminary
review by MOA
2. Preliminary review
1 Connections
by MOA
3. Feeding test and
Feeding test
4 Preparation and safety test
Safety test
4. Evaluation 4 100
Evaluation
5. Quality test 4 Experience
6. License approved 1 Speed
Quality test
Total 18 600
①The" Months" is the time the whole registration will take from the beginning
to the end. License approved
② "Hours" is the time I will spend on this registration.
12. Responsible authorities
1. MOA (Ministry of Agriculture):
Issues the registered license for import veterinary
drugs (import and local products)
2. China Institute of Veterinary Drugs Control
(CIVDC)
The Veterinary Drug Evaluation Institute
Quality trial
13. Registration procedures
Registration TIME
How we help Dossier
procedures Months Hours
preparation
1. Dossier
4 700 Organization
preparation
Preliminary
2. Preliminary review by MOA
review by MOA and 6 Connections
CIVDC
Clinical trials and
3. Clinical trials and residue tests
8 Preparation
residue tests
200
4. Evaluation by Evaluation
Veterinary Drugs 6 Connections
Evaluation Institute
5. Quality test 5 Experience Quality test
6. License approved 2 Speed
Total 31 900
NB: ①The" Months" is the time the whole registration will take from the beginning License approved
to the end.
②The "Hours" is the time I will spend on this registration.
16. Barriers for registration
• Dedicated team in Beijing office
• We have helped XX companies register products.
Lack of Experience • Experienced support for MNC globally
• Based in Beijing, China, AAC registration & support team of 8 trained
specialist in Intensive livestock industry.
Language • Chinese is our team’s 1st language and we are fluent in english
• Our china presence and reputation offers leverable opportunities for new
entrants.
• Our Team members have Animal Science, Veterinary and Masters
Culture/Connections qualifications in our industry, we understand the science and the technology