Quality Control & Regulatory Compliance

Our Quality: Manufacturing & Compliance Standards

In-house R&D, controlled batch production, testing, batch traceability, and product release under audited ISO 9001, ISO 22716 Cosmetics GMP, Halal, RSPO, and US MoCRA facility requirements in Rawang, Malaysia.

Cosmetic formulation scientist conducting R&D testing at HE Manufacturing lab

In-House R&D Capabilities

Formulation & Stability Laboratory

Our internal research and development team formulates, verifies, and tests custom personal care products, fragrances, and packaging compatibility long before commercial-scale manufacturing begins. By housing full stability and preservative efficacy testing under one roof, we eliminate third-party delays and secure strict formulation IP protection.

  • 5-Condition Accelerated Stability Testing
  • Preservative Efficacy Testing (PET)
  • Microbiological Challenge Testing
  • Packaging Compatibility & Leakage Testing

Controlled Batch Manufacturing

Scalable Batch Production Capability

Whether executing pilot orders for emerging brands or full-container commercial batches for global hotel chains and retail distributors, every production line operates under unified GMP quality protocols. Batch sizes flex by formulation format and container closure system without compromising analytical precision.

"Every batch manufactured at our Rawang plant adheres strictly to ISO 22716 Cosmetics GMP standards, ensuring full product integrity, lot-level traceability, and export documentation accuracy across international borders."
Industrial stainless steel mixing tanks for cosmetics batch production

Verified Global Compliance

Built on Audited Quality Standards

Our manufacturing facility in Selangor, Malaysia maintains active certifications audited by recognized international standard bodies, offering buyers seamless entry into regulated global markets.

ISO 9001 Quality Management ISO 22716 Cosmetics GMP JAKIM Halal Certified RSPO Sustainable Palm Member US MoCRA Facility Registered NPRA MOH Malaysia Certified Eco-Formulation Compliant

Certificates on File

Official audit certificates verifying our facility operational compliance. Signatures and verification codes are masked online for security; unredacted copies and Certificates of Analysis (CoA) are available upon project scoping.

ISO 22716:2007 Cosmetics GMP Certificate Audit document

ISO 22716:2007

Cosmetics Good Manufacturing Practices issued by FrenchCert UK Ltd.

Valid Until 20 Feb 2027
ISO 9001:2015 UKAS Quality Management Certificate document

ISO 9001:2015 (UKAS)

Quality Management System accredited by Bureau Veritas UKAS.

Valid Until 29 Jan 2027
ISO 9001:2015 Standards Malaysia Certificate document

ISO 9001:2015 (DSM)

Quality System Certification accredited by Standards Malaysia.

Valid Until 29 Jan 2027
GMP Compliance Certificate issued by MOH Malaysia NPRA

GMP Compliance

Issued by National Pharmaceutical Regulatory Agency (NPRA), Ministry of Health Malaysia.

Cert No. 3771/25

End-to-End Quality Assurance

4-Stage Quality Control Protocol

Every product batch undergoes continuous inspection and analytical verification from raw material quarantine to finished goods release.

Pre-production raw material identity and purity testing in lab

Stage 01 · Pre-Production

Raw Material Testing & Quarantine

Raw ingredients undergo purity verification, active assay verification, and microbiological screening before release into active production inventory.

In-process cosmetics quality control checking pH, viscosity, and density

Stage 02 · In-Process

In-Process Quality Control (IPQC)

Viscosity, pH balance, specific gravity, micro-emulsion integrity, and visual clarity are continuously monitored at defined compounding checkpoints.

Finished product cosmetics inspection and batch CoA release

Stage 03 · Post-Production

Finished Product Analytical Verification

Final filled containers undergo weight verification, Torque-test bottle sealing, batch code inspection, and final micro-plate sterility approval.

Controlled warehouse storage and batch lot inventory management

Stage 04 · Logistics & Storage

Controlled Environmental Storage

Finished goods are stored in climate-monitored warehouse zones prior to palletization, container loading, and global shipping dispatch.

Batch traceability and regulatory document compilation

Regulatory Compliance

US & EU Market Compliance Dossiers

Complete documentation support including Product Information Files (PIF), Safety Assessments (CPSR), INCI lists, and US MoCRA facility details.

Export carton packaging and container dispatch

Global Dispatch

Export Inspection & Certificate of Analysis

Every commercial export shipment includes batch-specific Certificates of Analysis (CoA) and customs documentation tailored for target import ports.

Technical Insight & Governance

Regulatory Standards & Quality Governance

Detailed insights into our quality laboratory practices, ISO 22716 operational audits, and Halal cosmetics manufacturing protocols across Asia.

Raw Material to Finished Bottle Testing

Comprehensive analytical protocols covering raw material validation, active ingredient concentration verification, and stability profiling in cosmetic contract manufacturing.

ISO 22716 Cosmetics Factory Audit Mandates

Understanding the critical requirements of ISO 22716 GMP certification for cosmetics factories, including sanitation controls, water purification loops, and batch record retention.

Halal-Certified Personal Care Manufacturing

Strict compliance guidelines for JAKIM Halal cosmetic manufacturing, detailing alcohol-free processing, porcine-free ingredient sourcing, and cross-contamination prevention.

Frequently Asked Questions

Quality & Compliance Standards, Explained

What certifications does HE Manufacturing hold?

ISO 9001, GMP Certified, Halal Certified, RSPO Member, US MoCRA Facility Registered, ISO 22716 Cosmetics GMP, and Eco-Formulation. Together these cover quality management, cosmetics GMP practices, Halal compliance, sustainable palm sourcing, and US facility registration. Registration does not imply FDA approval or endorsement.

How many quality control checkpoints does a product go through?

Four dedicated in-house stages: raw material quarantine testing before production, in-process quality control (IPQC) during compounding, finished product analytical verification after filling, and controlled environmental storage prior to dispatch.

Is formulation and stability testing done in-house or outsourced?

All formulation, fragrance development, packaging compatibility testing, preservative efficacy testing (PET), and 5-condition accelerated stability testing are performed entirely in-house at our Rawang, Malaysia facility.

Does batch size affect the quality control process?

No. Every order volume — from pilot brand trials to full-container shipments for multinational distributors — follows identical GMP quality control protocols, batch record logging, and analytical release criteria.

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