QUALITY ASSURANCE

Quality Assurance Documentation, for the batch file

Quality requirements are defined around the product specification, raw materials, production process and destination market. Depending on the project and available records, documentation may include ingredient information, SDS/MSDS, batch-specific COA and applicable quality or manufacturing records. Confirm the document set for the selected SKU or batch rather than assuming every document is available for every product.

Quality inspection area at the cosmetics manufacturing site

Quality control is part of every production handoff

Prink cosmetics coordinates commercial intake while manufacturing runs at the Baiyun site shared with Guangzhou Yuanxu Pharmaceutical Co., Ltd. Quality work covers incoming checks, in-process control, finished inspection and the documents buyers request when batch records exist.

Quality control benches and inspection tools

01 · Release

How quality control runs on an order

Each project confirms the inspection points that match the formula, pack and destination market.

  • Batch traceability

    Materials and bulk lots are tracked so release decisions can reference the production record.

  • Inspection and release

    Checks follow the agreed standard before bulk ships in drums or as filled units.

  • Document pack for export

    When records exist, buyers can request COA, SDS/MSDS, INCI and related shipping files.

Certification display area at the manufacturing site

02 · Certificates

Site certifications (SGS)

The manufacturing site holds the following SGS certificates. The certificate holder is Guangzhou Yuanxu Pharmaceutical Co., Ltd. Guangzhou Prink International Cosmetics Co., Ltd. uses this site; the two companies are separately registered and are not merged.

  • ISO 22716:2007

    SGS certificate CN21/31217 for Cosmetic GMP (ISO 22716:2007). Valid 18 July 2024 to 17 July 2027. Holder: Guangzhou Yuanxu Pharmaceutical Co., Ltd.

  • US FDA CFSAN Cosmetic GMP

    SGS certificate CN21/31218 for US FDA CFSAN Cosmetic GMP Guidelines (2008). Valid 18 July 2024 to 17 July 2027. Holder: Guangzhou Yuanxu Pharmaceutical Co., Ltd.

Documents buyers commonly request

Availability depends on the batch. The list below is a service capability, not an attachment on every product page.

  • COA
  • SDS / MSDS
  • INCI
  • Technical data / TDS when prepared for the order
  • Packing list and commercial invoice

Ask for documents on your next order

Tell us the product, destination market and which files you need for intake. For plant photos and filling scope, see Manufacturing Capabilities.