01Name the intended product accurately
Record fragrance format, declared concentration or product type, nominal fill, intended user, selling channel and destination. Do not infer eau de parfum, natural, hypoallergenic, long-lasting or other claims from scent strength or supplier language without a defined basis.
02Assign a controlled formula reference
Use a formula, compound or supplier reference with version and date, and link it to the approved liquid sample. Record intended color and allowed appearance range. A fragrance name can remain unchanged while composition, concentration or ingredient source changes.
03Request documents by business role
Ask what formulation information, safety data, allergen or ingredient information, IFRA-related documentation, manufacturing records, transport classification and destination files are available for the exact version. The required package depends on product, jurisdiction, buyer role and route, so use qualified regulatory and dangerous-goods review.
04Evaluate the sensory sample blind
Code samples so reviewers are not led by name, package or price. Record first impression, development, wear condition, strength and difference from the brief at fixed intervals. Sensory observations guide selection but do not establish chemical composition, safety or a universal longevity claim.
05Approve the complete packaging system
Control bottle, decoration, pump, collar, cap, gasket, dip tube, label, carton, insert, cellophane or seal and shipping protection. Review spray, leakage, evaporation, fit, finish and printed information using filled production-equivalent samples.
06Create batch and retention records
Define batch code location and format, filling date, formula version, component lots and finished quantity. Agree retention samples and storage. A batch record supports traceability; it does not replace testing, market notification or conformity work required for the destination.
07Control transport, launch and reorder
Confirm classification, packaging, marks, documents and carrier acceptance for the actual liquid and route with qualified providers. At reorder, review formula, raw material, color, facility, bottle, pump, artwork and regulations for change before relying on the previous approval.