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QUALITY & DOCUMENTATION
Selected certificates, licences and registration records are presented with their stated scope and validity so buyers can begin due diligence from documented evidence.
INTERNATIONAL SYSTEMS
These documents support supplier assessment within their stated scopes. They do not create a universal product approval, registration or right to sell in every market.
Open document image INTERNATIONAL SYSTEM
Solid pet additive premix feed. The certificate states that the programme is modelled after U.S. FDA 21 CFR Parts 111 and 507.
Open document image INTERNATIONAL SYSTEM
Audited scope covers animal supplement soft chewable tablets and the processes listed on the two-page certificate.
Open document image INTERNATIONAL SYSTEM
Processing of solid pet additive premix feed packed in PET bottles, within the process scope stated on the certificate.
Open document image QUALITY MANAGEMENT
Veterinary drug production within the scope of the applicable licence.
Open document image REGISTRATION RECORD
Foreign food facility registration for animal food / pet food. Registration does not mean FDA product approval or endorsement.
CHINA QUALIFICATIONS
The original Chinese-language documents are shown as documentary evidence. Their scope is described conservatively in English and should be checked against the source image.
Open document image CHINA QUALIFICATION
Chinese Good Manufacturing Practices for Animal Drugs within the inspection scope stated on the certificate.
Open document image CHINA QUALIFICATION
Production licence covering the dosage forms and production scope listed in the original Chinese document.
Open document image CHINA QUALIFICATION
Solid pet additive premix feed within the product scope stated on the licence.
Open document image CHINA EXPORT REGISTRATION
Registration for an establishment producing, processing or storing additive premix feed for export.
BUYER DUE DILIGENCE
Quality evidence is matched to the product, facility, dosage form, packaging route and destination market under discussion.
Confirm that the certificate or licence actually covers the relevant facility, product type and production activity.
Align formulation, dosage form, product specification, testing expectations and buyer documentation.
Send classification, claims, label, registration and permitted-use questions to qualified destination-market reviewers.
START A CONVERSATION
Share the product, dosage form and destination market. We will organise the relevant available documents for buyer review.