B2B Technical Dossier VaultLot-Specific SubstantiationShenzhen Factory Direct

Technical Compliance & Regulatory Dossier Vault

Direct laboratory substantiation for beauty brand founders, purchasing directors, and regulatory affairs toxicologists. Review authentic testing parameters, instrument methodologies, and statutory compliance frameworks. All dossiers are presented with watermarked specimen previews; submit your project details to unlock unredacted PDFs.

Flexible MOQ

100 units

per shade / formula

Fast Lab Sampling

3–7 days

100% credited to bulk

Bulk Lead Time

25–35 days

DDP air / sea delivery

Reply SLA

1 Business Day

dedicated chem desk

Browse 5 Technical Dossiers ↓WhatsApp Compliance Chemist

Verified Laboratory & Regulatory Dossier Catalog

Each dossier module below features an interactive watermarked specimen preview illustrating our real test methodologies, instrument limits, and reference standards. Select any dossier to request the full, unredacted laboratory package.

Heavy Metal SafetyRef: DOC-ICP-2026

ICP-MS Trace Elemental Analysis Dossier

California Prop 65 Safe Harbor Toxicological Support

Quantitative elemental analysis profiling Lead (Pb), Arsenic (As), Cadmium (Cd), and Mercury (Hg). Designed to provide brand toxicologists with the batch data needed for California Proposition 65 safe harbor exposure assessments.

Analytical Instrument:Agilent 7800 Quadrupole ICP-MS

Testing Standard:EPA 3052 Microwave Acid Digestion

Technical Highlights:

✓EPA 3052 closed-vessel fluoropolymer microwave digestion
✓High-matrix introduction system with octopole collision cell (He mode)
✓Sub-ppb limit of quantitation (LOQ) precision
✓Lot-specific COA testing upon release

OFFICIAL SPECIMEN · REDACTED FOR B2B REVIEW

LABORATORY SPECIMEN CERTIFICATE

DOC-ICP-2026

Analyte / Evaluation Point	Standard Reference	Test Result	Status
Lead (Pb)	Prop 65 MADL/NSRL Benchmark	Pass / Below Safe Harbor	VERIFIED
Arsenic (As)	Prop 65 Inhalation/Ingestion Limit	Pass / Below Safe Harbor	VERIFIED
Cadmium (Cd)	Prop 65 Maximum Allowable Dose	Pass / Below Safe Harbor	VERIFIED
Mercury (Hg)	FDA 21 CFR Cosmetic Trace Limit	Pass / Below Limit	VERIFIED

Sign-off: Laboratory Quality Assurance DeskFull unredacted batch PDF available on request

Fragrance & Essential OilsRef: DOC-IFRA-51

IFRA 51st Amendment Fragrance Safety Report

Quantitative Risk Assessment (QRA2) for Category 5A/5B

Comprehensive dermal safety review of fragrance oils and natural essential oil blends. Verifies maximum permissible concentration limits for Category 5A (body lotion) and 5B (face moisturizers), plus phototoxic furanocoumarin restrictions.

Analytical Instrument:GC-MS Headspace / HPLC Allergen Screen

Testing Standard:IFRA 51st Amendment Standards & QRA2 Dossier

Technical Highlights:

✓Full certificate of compliance signed by fragrance master chemists
✓Dermal sensitization thresholds calculated per consumer surface area
✓Zero animal testing in fragrance compound sourcing per California SB 1249
✓Custom allergen-free and clean-beauty fragrance library available

OFFICIAL SPECIMEN · REDACTED FOR B2B REVIEW

LABORATORY SPECIMEN CERTIFICATE

DOC-IFRA-51

Analyte / Evaluation Point	Standard Reference	Test Result	Status
Category 5A (Body Shimmer Oil)	IFRA 51st Dermal Threshold	100% Within Safe Threshold	VERIFIED
Category 5B (Face/Setting Mist)	IFRA 51st Facial Application	100% Within Safe Threshold	VERIFIED
Phototoxic Furanocoumarins	Bergapten / Citrus Restriction	ND / Safe for Sun Exposure	VERIFIED
26 EU Cosmetic Fragrance Allergens	EC 1223/2009 Annex III	Fully Disclosed on Labeling	VERIFIED

Sign-off: Laboratory Quality Assurance DeskFull unredacted batch PDF available on request

North America ComplianceRef: DOC-MOCRA-2024

US FDA MoCRA 2024 Product & Facility Listing Checklist

Statutory Technical Data for US Market Commercialization

Turnkey technical specifications and manufacturing disclosures needed by US Responsible Persons (RP) to complete cosmetic facility registrations, annual product listings, and statutory adverse event handling.

Analytical Instrument:FDA Cosmetics Direct Integration Data Package

Testing Standard:FD&C Act Modernization of Cosmetics Regulation Act (MoCRA)

Technical Highlights:

✓Statutory disclaimer: FDA does not certify or license cosmetic contract plants
✓Complete INCI percent ranges provided under mutual NDA for legal counsel review
✓Batch traceability and lot coding protocols for US retail compliance
✓Full DDP customs clearing support with FDA cosmetic tariff classifications

OFFICIAL SPECIMEN · REDACTED FOR B2B REVIEW

LABORATORY SPECIMEN CERTIFICATE

DOC-MOCRA-2024

Analyte / Evaluation Point	Standard Reference	Test Result	Status
Facility Registration Info	Section 607(a) Mandatory Preparation	Factory Data Pack Available	READY
Product Ingredient Listing (SPL)	Section 607(c) Formulation Filing	Exact INCI Breakdown Provided	READY
Safety Substantiation Dossier	Section 608 Adequate Substantiation	Toxicological Rationale Ready	READY
Adverse Event Reporting Contact	Section 605 Contact Routing	RP Labeling Integration Ready	READY

Sign-off: Laboratory Quality Assurance DeskFull unredacted batch PDF available on request

Europe & UK ComplianceRef: DOC-EU-CPNP

EU Regulation (EC) 1223/2009 & UK SCPN Dossier Package

Cosmetic Product Safety Report (CPSR Parts A & B) Foundation

Technical documentation architecture to support European and British Responsible Persons in compiling the Product Information File (PIF) and uploading notifications to the EU CPNP and UK SCPN portals.

Analytical Instrument:CPSR Toxicological Risk Assessment Framework

Testing Standard:Regulation (EC) No 1223/2009 & UK Cosmetic Regulation

Technical Highlights:

✓Formula composition breakdowns formatted for EU Safety Assessors
✓Lot-specific COA testing upon release with full physicochemical specs
✓Coordination with leading European compliance consultancies and Eurofins partners
✓Cruelty-free formulation verification complying with EU animal testing bans

OFFICIAL SPECIMEN · REDACTED FOR B2B REVIEW

LABORATORY SPECIMEN CERTIFICATE

DOC-EU-CPNP

Analyte / Evaluation Point	Standard Reference	Test Result	Status
CPSR Part A (Safety Information)	EC 1223/2009 Annex I Part A	Formula & Stability Data Pack	VERIFIED
Microbiological Quality Specs	USP <61>/<62> / ISO 17516 Guidelines	Harmonized Testing Limits	VERIFIED
Preservative Challenge Profile	ISO 11930 Efficacy Verification	Standardized Challenge Pack	VERIFIED
Packaging Interaction / Leachables	Food-Grade Contact Safety	Virgin Glass & PET Compliance	VERIFIED

Sign-off: Laboratory Quality Assurance DeskFull unredacted batch PDF available on request

Eco-Friendly & Microplastic FreeRef: DOC-PLANT-GLITTER

Plant-Cellulose Biodegradable Glitter Testing Summary

ISO 14851 Freshwater Aquatic Aerobic Biodegradability

Independent technical substantiation proving that our eco glitter line utilizes plant-derived regenerated cellulose rather than microplastic polymers, fully exempt from the EU 2023/2055 microplastics ban.

Analytical Instrument:Respirometric Aquatic Biodegradation Chamber / FTIR Spec

Testing Standard:ISO 14851 / OECD 301B Protocol Alignment

Technical Highlights:

✓100% plant-cellulose derived core substrate from sustainably harvested wood pulp
✓Marine and freshwater degradation profiles for reef-safe formulations
✓Precision optical refractive coating without synthetic microplastic film
✓Solvent-resistant performance in water-based and lipid suspension bases

OFFICIAL SPECIMEN · REDACTED FOR B2B REVIEW

LABORATORY SPECIMEN CERTIFICATE

DOC-PLANT-GLITTER

Analyte / Evaluation Point	Standard Reference	Test Result	Status
Freshwater Biodegradability	ISO 14851 Aerobic Protocol	≥60% Biodegradation in 28 Days	PASS
Polymer Classification	EU Regulation 2023/2055 Review	Natural Polymer / Non-Microplastic	EXEMPT
Heavy Metal Purity	Cosmetic Colorant Purity Specs	Lot-Specific ICP-MS Compliant	PASS
Ocular & Dermal Particle Edge	Precision Micro-Die Precision Cut	Smooth Hexagonal Safety Edge	VERIFIED

Sign-off: Laboratory Quality Assurance DeskFull unredacted batch PDF available on request

Frequently Asked Technical & Compliance Questions

Can I share these dossiers directly with my brand's safety toxicologist?›

Yes. The unredacted PDF packages include analytical methodology details, limit-of-detection data, calibration curves, and full INCI concentration ranges designed specifically for board-certified toxicologists compiling cosmetic safety assessments (CPSR / MoCRA).

Do these lab tests cover custom shades and proprietary scents?›

The base dossiers cover our standard benchmark formulas. When you order custom pilot sampling (100 units MOQ), our laboratory conducts lot-specific COA testing and generates tailored IFRA/allergen sheets for your exact fragrance percentage and pigment combination upon release.

What is your policy regarding animal testing and cruelty-free claims?›

All formulations are developed without animal testing in strict alignment with California SB 1249 and EU Regulation (EC) 1223/2009. We provide signed declarations verifying cruelty-free formulation to support your brand's Leaping Bunny or PETA verification filings.