GMP Certified Manufacturing in Cavite
Good Manufacturing Practices (GMP) certification ensures cosmetics are manufactured under controlled, documented, and verified processes. Orsolab Inc. is a GMP-certified cosmetics manufacturer in Tanza, Cavite holding FDA Cosmetics LTO No. LTO-3000006301418 and HUHS License No. CCHUHSRR-REGIVA-HUHSM-1695.
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GMP Certification Requirements
Philippine FDA requires cosmetics manufacturers to implement GMP covering: personnel hygiene and training, building and facilities design and maintenance, equipment qualification and calibration, production and process controls, quality control systems and testing, complaint handling and product recalls, documentation and record keeping, supplier qualification and raw material controls.
Orsolab maintains GMP compliance verified through regular FDA inspections and internal audits. Documentation available for brand due diligence and facility audits.
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Why GMP Matters for Brands
Brands benefit from GMP-certified manufacturing through: consistent product quality batch-to-batch, reduced contamination and safety risks, documented traceability for recalls if needed, FDA compliance for distribution and retail, audit-ready documentation for investors or retail partners, export readiness for international markets.
See Contract Manufacturing Philippines and How to Choose a Contract Manufacturer.
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Location: Tanza, Cavite
Orsolab's GMP-certified facility is located in Tanza, Cavite — 45 minutes from Manila via CAVITEX. The facility produces skincare, haircare, body care, and household products. Brands are welcome to visit by appointment. Learn more at Tanza Cavite Manufacturer.
Submit inquiry to discuss your requirements and GMP documentation needs.
FAQs
What is GMP certification?
Good Manufacturing Practices (GMP) certification verifies that cosmetics are manufactured following documented, controlled processes ensuring quality and safety.
Is GMP required in the Philippines?
Yes. FDA requires cosmetics manufacturers to implement GMP. Orsolab holds FDA Cosmetics LTO No. LTO-3000006301418 with verified GMP compliance.
Can I audit the facility?
Yes. Brands are welcome to conduct facility audits by appointment. GMP documentation available for review.