For fragrance buyers and brand managers, ISO 22716 (Cosmetics GMP) is not just a certification—it’s the framework proving that a facility can consistently produce safe, traceable, and compliant fragrance bases and finished goods. Understanding what to audit and verify ensures your brand avoids compliance gaps and costly recalls while protecting claim integrity.
Why ISO 22716 Matters in Fragrance Procurement
- Consistency: Ensures every batch matches approved sensory, color, and compositional standards.
- Safety assurance: Aligns with cosmetic regulation in the US, EU, and other major markets.
- Traceability: Full documentation of raw materials, processes, and packaging components.
- Audit readiness: Demonstrates control to brand partners, retailers, or regulatory agencies.
Core Documentation to Review Before Approval
- Valid ISO 22716 certificate (issued by an accredited body).
- GMP procedural manual and staff training records.
- Batch records with traceable raw material lot numbers.
- Microbiological and stability test summaries.
- Packaging compatibility test reports (especially for alcohol-based perfumes).
- Supplier qualification records for essential oil and aroma-chemical vendors.
Key GMP Audit Focus Points for Fragrance Buyers
1. Raw Material Handling
- Check storage segregation for aroma oils, alcohols, and allergens.
- Request incoming material COAs, allergen declarations, and IFRA compliance certificates.
- Verify calibration of weighing and mixing equipment.
2. Production and Filling
- Ask for documented cleaning validation for blending tanks and filling lines.
- Inspect filling area for environmental controls preventing contamination.
- Ensure pump systems are alcohol- and fragrance-compatible (elastomer grade review).
3. Laboratory Controls
- Confirm sensory evaluation is standardized (panel test or GC interface method).
- Request chromatograms or spectral fingerprint summaries for identity check.
- Review stability storage conditions (temperature/humidity tracking).
4. Label, Batch Coding, and Traceability
- Every batch should be traceable to ingredient lots and operator records.
- Check barcode or batch code sequencing for recall readiness.
- Ensure labeling matches regulatory wording formats for target market.
Quick Reference: What to Verify During a Site Visit
| Area |
What to Verify |
Evidence Type |
| Raw Materials |
COA, storage temperature logs |
COA / Audit logbook |
| Mixing Area |
Tank sanitation records |
Cleaning validation |
| Filling Line |
Operator GMP training |
Training certificate |
| Finished Product |
Stability and micro test reports |
Lab reports / QC sign-off |
| Packaging |
Alcohol-resistance test for sprayer bottle |
Compatibility report |
Common Audit Gaps to Prevent
- Expired ISO certificate: Always verify validity and scope.
- Incomplete batch records: Request random samples to test record accuracy.
- Cross-contamination: Shared filling lines without validated cleaning between fragrance types.
- Labeling mismatch: Translation errors or unapproved phrases in EU/US claims.
- Poor packaging compatibility: Leaks or degraded pumps in alcohol-heavy formulas.
Buyer FAQ
What’s the difference between ISO 22716 and regular factory audits?
ISO 22716 focuses on manufacturing control and documentation under Good Manufacturing Practice. A general audit may only check capacity or appearance—it won’t prove process discipline.
Do all fragrance manufacturers need ISO 22716?
Not required by law everywhere, but in markets like the EU and UK, it’s strongly expected for cosmetic-grade products. Major retailers often make it mandatory.
How often should a buyer reverify compliance?
At least every 12 months or after any regulatory, formulation, or capacity change impacting GMP status.
How can I confirm a certificate is real?
Cross-check the issuing body on official accreditation directories and ensure the site address matches your manufacturer’s exact location.
Should I test fragrance stability myself?
Yes, especially if the product will be repacked or used in different bottles than tested by the manufacturer. Request the original stability protocol and duplicate testing under your conditions.
Request a Quote for ISO 22716-compliant fragrance manufacturing support. Provide your target market, fragrance type, batch size, and packaging format for a precise response.
Hi, I'm Alex Zong, hope you like this blog post.
With more than 20 years of experience in OEM/ODM/Private Label Cosmetics, I'd love to share valuable knowledge related to cosmetics & skincare products from a top-tier Chinese supplier's perspective.