At ProTech Health Sciences, we guarantee uncompromising standards across every stage of OEM production. Leveraging 20+ years of manufacturing experience, state-of-the-art cleanroom technology, and strict quality control protocols, we empower global brands with safe, consistent, and market-compliant health supplements, skincare, and functional food products.
Our production facility operates under standardized Quality Management Systems (QMS), integrating automated processing, micro-testing, and raw material validation. Every batch manufactured in our facility undergoes rigorous physical, chemical, and microbiological testing to ensure absolute safety, potencies, and shelf-life stability.
Whether you are launching private label nutraceuticals, advanced skincare formulas, or dietary supplements for global distribution, our technical infrastructure ensures full traceability from raw material sourcing to final export shipping.
Our holistic quality control structure mitigates risk, enforces regulatory compliance, and protects brand reputation.
Comprehensive SOP execution aligned with cGMP, ISO 22000, and HACCP guidelines. Real-time batch recording and systematic continuous improvement procedures.
Strict auditing of raw material vendors, rigorous identity verification, heavy metal screening, and micro-contamination prevention before materials enter production.
State-of-the-art cleanroom environment monitoring (ISO 8 / Class 100,000), automated dosage precision, temperature/humidity controls, and continuous parameter logging.
In-house quality control testing for batch uniformity, dissolution rates, microbial safety, active component potency, and physical seal integrity across all SKUs.
Ongoing technical skill certification, cleanroom hygiene protocol compliance, and continuous training for our operational team and chemists.
Periodic internal quality audits, formula stability validation, CAPA implementation, and optimization of yield efficiencies to minimize batch variability.
From raw ingredient quarantine to final Certificate of Analysis (CoA) issuance, our products follow a strict 5-stage verification roadmap.
Quarantine, sampling, species/ingredient verification, and microbial testing.
Monitoring weight variation, moisture, hardness, blending uniformity, and liquid viscosity.
Heat-seal testing, fill-volume verification, leak detection, and label compliance checks.
Comprehensive third-party and internal lab analysis issuing official Certificate of Analysis.
Climate-controlled warehousing, tamper-evident palletizing, and global export documentation.
Consult with our quality assurance experts and formulation team today. Get full technical dossiers, facility audit access, and sample quotes tailored to your market.
