We coordinate factory certifications, third‑party tests, and market‑specific dossiers for export. This is general guidance only — confirm the latest rules with your compliance advisor.
Good Manufacturing Practices covering facilities, personnel, and records.
US‑focused GMP frameworks and facility registrations.
Quality management / social responsibility; audit reports available (partially redacted).
Responsible Person (RP) appointment and CPNP notification.
PIF with safety assessment, stability & challenge tests.
Label in required languages; claims substantiation.
Facility registration, product listing, adverse event recordkeeping.
INCI listing, label review, safety file.
Retailer/platform‑required third‑party testing.
UK Responsible Person; SCPN submission; UK label requirements.
Local registrations and permitted lists; Arabic/Spanish/Portuguese labels.
Routine limits & challenge tests.
3/7/28 days; 40°C/RH75%; formula × pump/bottle/gasket compatibility.
Critical elements and sensitizers; safety evaluation.
Batch COAs, safety sheets, and fragrance compliance.
Legal elements and layout checks.
Batch, raw materials, packaging, and production records.
Tell us the destination market and launch date — we’ll map samples, tests, and documents with lead‑times.