Regulatory Control Facility : Ready For Global Market
Regulatory Compliances Facilities
Our Responsible Sourcing Program is backed by a dedicated regulatory control and compliance facility, ensuring every raw material and packaging input meets global quality and safety standards. We maintain full traceability across the supply chain, reinforcing ethical and compliant procurement practices. supporting consistent quality and market readiness worldwide. By combining ethical sourcing with regulatory precision, we provide brands with verified, compliant and trustworthy.
Comprehensive Quality Compliance Framework
Raw Material Verification
- Source Authentication – GACP-certified farms and USP/EP-compliant suppliers.
- Safety Screening – Testing for heavy metals, pesticides, microbiological contaminants, and allergens.
- Advanced Testing – HPLC, GC-MS, FTIR for botanical and chemical profiling.
In-Process Quality Control
- Continuous monitoring of critical control points (CCPs) during manufacturing.
- In-process sampling for potency, blend uniformity, and microbial safety.
- Automated alerts for real-time corrective actions.
Finished Product Quality Checks
- Potency Verification – Ensuring label claim accuracy.
- No Use of Invalid Symbols & Miss Guiding Pictures on label
- Shelf Life Stability Studies – Real-time and accelerated conditions up to 60 months.
- Packaging Integrity Testing – Leak detection, seal validation, and barrier performance.
Raw Material Verification
In- Process Testing
Finish Quality Checks
Regulatory Compliance Capabilities
International Standards & Certifications
- WHO-GMP, ISO 22000, ISO 22716.
- HACCAP & Kosher Certification.
- Organic Certification – USDA, EU, and India Organic.
Global Regulatory Alignment
- US FDA 21 CFR 111/210 – Dietary supplements and cosmetics.
- EU Cosmetic Regulation (EC 1223/2009) – Safety assessments and PIF creation.
- TGA (Australia), ASEAN, GCC – Product registration and compliance.
Regulatory Documentation & Market Entry Support
Export-Ready Documentation
- Certificate of Analysis (COA).
- Stability data and safety reports.
- Product registration dossiers.
Country-Specific Compliance
- Ingredient legality verification per target market.
- Health claims validation under local laws.
- Support for FDA, EFSA, GCC, and TGA submissions.
Laboratory Capabilities
- Analytical chemistry labs for actives quantification.
- Microbiology labs for pathogen detection.
- Stability chambers with climate control for various zones (ICH guidelines).
LyonsBarry’s Quality Compliance & Regulatory Facility
Zero-Compromise Quality Policy – Ensuring safety and effectiveness in every product.
Audit-Ready – Facilities and records maintained for immediate inspection by global authorities.
Expert Regulatory Team – Specialists in multi-market compliance and documentation.
Global Market Readiness – Products fully prepared for entry into 85+ countries.
