Use this to pre-qualify manufacturers: what to ask for, what to review, and what to treat as a red flag.
ISO 22716 (Cosmetic good manufacturing practice) is the internationally recognized standard for cosmetic production. This checklist is based on the standard’s requirements and common buyer due diligence: certificates and scope, quality controls, traceability, change control, and complaint handling. Use it before requesting quotes to filter for GMP-ready partners.
Certificates: ISO 22716 certificate (scope + site address), audit date, and any GMP certifications.
Quality controls: batch record approach, in-process controls, microbiological controls (as applicable), and release criteria.
Traceability: raw material supplier traceability, lot tracking, retention samples, and recall process.
Change control: how formula, packaging, and process changes are approved and communicated.
Complaints: complaint handling, investigations, CAPA process, and trend reviews.
Subcontracting: which steps are in-house vs subcontracted (testing, packaging sourcing, fill/pack lines).
Certificate scope does not cover the relevant product types/processes; unclear subcontracting; weak documentation; unwillingness to share core QA details under NDA.
Yes. Use the ISO 22716 browse page or request quotes and ask manufacturers to confirm certification scope.
No. It addresses GMP practices. Compliance for EU/UK markets may still require labeling review, notifications (CPNP/SCPN), and a Responsible Person.
ISO 22716:2007 (Cosmetics — Good Manufacturing Practices) is available from ISO. This checklist summarizes key areas buyers typically verify; for full requirements, refer to the standard or an accredited certification body.
Cruxi does not provide legal or certification advice. Verify certification scope and QA with manufacturers directly.
Want ISO 22716-aware quotes?
Request quotes and ask for certification scope and QA controls.
