Quality Assurance

Quality is verified, not assumed

An in-house laboratory, documented inspection protocols and premium raw materials keep every batch consistent — from the first container to the hundredth.

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In-House QA Laboratory Testing Simulator

Digital "Diaper Core Absorption" Lab Simulator

Experience our 5-layer absorption technology virtually. Select product specification, inject fluid volume, and benchmark instant strike-through and rewet dryness against ISO 11948-1 standards.

Ready for Testing · Standby Mode

0.0s
Layer 1: 3D Diamond Embossed Hydrophilic TopsheetInstant Liquid Pass
Layer 2: Acquisition & Distribution Layer (Emerald Green ADL)Channeling Layer
Layer 3: Sumitomo Super Absorbent Polymer (SAP) + Virgin Fluff CoreHigh-Capacity Polymer
Layer 4: 3D Hydrophobic Standing Cuff Leak GuardsDouble Elastic Barrier
Layer 5: Microporous Cloth-Like Breathable PE Film3450 g/m²/24h vapor release
Strike-Through SpeedStandard <10.0s
Rewet Under 2.5kgStandard <2.00g
Fluid RetentionStandard >90.0%
Breathability3450g/m²/24h
International Quality & Regulatory Compliance Hub

Certificates & Laboratory Test Dossier Verification

Our Bhiwandi manufacturing facility and hygiene product lines hold verified certifications required by international customs authorities, hospital tenders, and global retail chains.

Quality Management
Active & Verified

ISO 9001:2015 Quality Management System

TUV / Accredited Global Certification Body
Validity: Annual Surveillance Verified

Design, high-speed converting manufacturing, in-line optical QA, and worldwide maritime export of disposable baby diapers, adult incontinence diapers, and hygiene underpads.

ISO 9001:2015Batch TraceabilityDocument Control QMS
International Conformity
Active & Verified

CE European Conformity (MDR & Hygiene Directives)

European Authorized Representative & Notified Technical File
Validity: 2024 – 2027

Technical compliance for Class I hygiene products and adult incontinence medical devices under EU Regulation 2017/745 (MDR) and General Product Safety Directives.

EN ISO 14971 Risk ManagementEN ISO 10993 BiocompatibilityEU REACH compliant
Quality Management
Active & Verified

Good Manufacturing Practice (GMP) Hygiene Cleanroom

National Licensing Authority / FDA Maharashtra
Validity: Annual Surveillance Verified

Fully enclosed manufacturing facility with positive air pressure, HEPA filtration, automated insect traps, staff gowning airlocks, and microbial quarantine protocols.

Zero-Contamination AirlocksIn-Line Metal DetectionPositive Air Pressure
Medical & Clinical
Active & Verified

Dermatological Safety & Hypoallergenic Test Report

Independent Clinical Dermatological Research Laboratory
Validity: Annual Surveillance Verified

48-Hour Human Repeat Insult Patch Test (HRIPT) on sensitive human skin. 0.00 Primary Irritation Index, verified free of elemental chlorine, phthalates, parabens, and synthetic dyes.

0.00% Skin IrritationHypoallergenicChlorine-Free Core
Safety & Testing
Compliant

ISO 14001:2015 Environmental Management

Accredited Environmental Registrar
Validity: 2024 – 2027

Sustainable production management: zero chemical wastewater runoff, 100% baling and recycling of non-woven cutting scrap, and energy-efficient servo electric motors.

Zero Waste RecyclingEco-friendly MaterialsLow-Emission Converting
Safety & Testing
Active & Verified

SGS / Intertek Toxicological Safety Screening

SGS Testing Services / Intertek Global
Validity: Annual Surveillance Verified

Comprehensive multi-substance screening for SVHC (Substances of Very High Concern), heavy metals (Lead, Cadmium, Arsenic), organotins, and formaldehyde.

Heavy Metal FreeSVHC NegligibleRoHS Compliant Materials

Quality Pillars

Six checks behind every pack

Testing Laboratory

Absorbency, rewet, tensile strength and leakage testing on every production batch.

Inspection Process

Pre-production, in-line and pre-shipment inspections, open to third-party auditors.

Safety Standards

Skin-safe, dermatologically tested materials free from harmful substances.

Quality Control

Documented checkpoints at every stage with traceable batch records.

Premium Material

Imported SAP, fluff pulp and non-wovens from approved global suppliers only.

International Standards

Manufacturing and labelling aligned to destination market regulations.

Quality testing laboratory at Fair Deal Corporation

Manufacturing Process Control

Where quality is actually decided

Most product failures start at raw material and line settings — so that is where our controls are heaviest.

  • Supplier approval and incoming material certificates
  • Line parameter validation at every product changeover
  • Hourly in-process sampling with recorded results
  • Batch retention samples held for traceability
  • Final packing audit before warehouse transfer
  • Pre-shipment inspection with photographic record

Certifications & Compliance

Recognised quality standards

Documentation available on request for buyers, tenders and import clearance.

ISO 9001 Quality Management

GMP Compliant Manufacturing

CE Marked Product Ranges

Dermatologically Tested

SGS / Third-Party Inspected

Export Documentation Compliant

Quality Verification

Request our quality dossier or visit our facility

We share test reports, specification sheets and welcome pre-production plant audits by buyer inspection teams.