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Buyers searching for a GMP certified Chinese herb supplier should verify the certificate holder, manufacturing site, certificate or license number, validity, scope and issuing authority—not just the certificate logo. This page summarizes the manufacturing licenses, US FDA food-facility registration, HACCP certification and ISO management-system certificates supporting Aile Herb supply projects.
Supplier qualification should verify the certificate holder, manufacturing site, number, validity, scope and issuing body. The documents below cover the main manufacturing, food-safety and management-system credentials supporting the production facility. Buyers can also review the Chinese herb factory and manufacturing capability behind these credentials. To check whether a supplier actually manufactures the product or is a trading company, compare its business license with its drug or food manufacturing license, as explained in our guide to Chinese herb manufacturer vs trading company.

License No.: 甘20160045
Scope: TCM Decoction Pieces
Issued by: Gansu Provincial Drug Administration Valid Through: January 31, 2031
This license authorizes TCM decoction-piece manufacturing at the named production site within the stated scope. Applicable pharmaceutical GMP requirements form part of the manufacturing and regulatory framework.

License No.: SC10662080000998
Relevant Scope: Plant beverages, substitute teas
Issued by: Pingliang Market Supervision Administration
Valid Through: April 1, 2030
This license authorizes the listed food-product categories at the named production site. Buyers should confirm that the selected finished product falls within the applicable licensed scope.

Certificate No.: 001HACCP2600122
Issuing Body: China Quality Certification Centre (CQC)
HACCP certification covers the applicable food-safety hazard-control system for the certified site and scope. It supports supplier qualification but does not replace product-specific batch testing or buyer specifications.
ISO 9001 — Quality Management System
ISO 14001 — Environmental Management System
ISO 45001 — Occupational Health & Safety Management System
ISO 50001 — Energy Management System
ISO 9001 — 00126Q301476R001
ISO 14001 — 05126E00313R053
ISO 45001 — 05126S00291R053
ISO 50001 — GH003-2025En2420
These are management-system certifications for the certified site and scope. They support supplier qualification but are not product certifications and do not replace batch-specific quality evidence.
Registration No.: 15114561590 — The supporting production facility is registered with the U.S. Food and Drug Administration as a food facility. FDA registration is a facility registration; it is not FDA approval or endorsement of any product.
Manufacturing licenses and system certifications describe the approved site, management system and applicable production scope. They do not replace batch-specific product evidence. Every production batch is issued with a batch-specific COA and undergoes pesticide-residue and heavy-metal testing, while additional reports are confirmed according to the product and order requirements.

Food products and TCM decoction pieces fall under different manufacturing authorizations and quality requirements. Buyers should review the license that applies to the specific product they intend to purchase rather than treating “GMP” as one universal certificate.
Different product categories require different manufacturing authorizations. The applicable license should be confirmed according to the product being sourced.
Buyers carrying out supplier qualification can review available certificate copies, facility information and supporting quality documents. Live video review, third-party inspection or an on-site visit can be discussed according to the project stage, inspection scope and access requirements.
It means the supporting food-production facility is registered with the U.S. Food and Drug Administration as required for the applicable food-facility activity. FDA registration does not mean FDA approval, certification or endorsement of the facility’s products.
The China Food Production License applies to the food-product categories stated in its scope, while the NMPA Drug Manufacturing License applies to authorized pharmaceutical manufacturing such as TCM decoction pieces. Buyers should review the license that corresponds to the actual product being purchased.
Required licenses, certifications and documents depend on the product, destination market and buyer qualification procedure. Buyers commonly review the applicable manufacturing license, HACCP or quality-system certificates, facility registration where relevant, and batch-specific quality documents.
Yes. Available supplier-qualification documents can include current license and certificate copies, certificate numbers, issuing bodies, scope and validity information. Batch-specific quality documents are reviewed separately according to the product and order scope.
Verify the certificate or license holder, manufacturing site, number, issuing body, validity and product scope. Then separately review batch-specific quality evidence such as the COA and required testing records for the product you intend to purchase.
Request available copies of the manufacturing licenses and certifications relevant to your supplier review, together with certificate numbers, scope and validity information. Sample batch documentation can also be discussed according to your product and qualification requirements.