US Production Base
Our Springville, Utah facility delivers domestic lead times, zero tariff liability, and complete cGMP compliance under 21 CFR Part 111 & 117 for North American and overseas buyers.
Springville, Utah · FDA-Registered Facility
About PAG Pharmatech America
Premier US-based Contract Development and Manufacturing Organization (CDMO) delivering pharmaceutical-grade dietary supplement solutions to DTC brands, Amazon sellers, and global importers worldwide.
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Years CDMO Heritage
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Custom Formulations
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Dosage Form Platforms
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Continental Hubs
FDA-Registered Operations SQF Edition 9 & cGMP Full Batch Documentation & CoA Integrated Global Sourcing Export & Regulatory Ready
Our Story & Heritage
Bridging Global Scale with US Manufacturing Precision
PAG Pharmatech America LLC operates as the North American headquarters of PAG Group — a global CDMO founded in 1995 with manufacturing infrastructure spanning three continents and distribution reaching over 50 countries.
Pharmaceutical Standards
Every line operates under rigorous quality management systems. We conduct comprehensive analytical testing, active assay verification, and microbial screening for every batch.
Global Supply Redundancy
Integrated supply chain nodes in Utah, Europe, and Asia protect client brands from raw material bottlenecks and single-region supply disruptions.
Manufacturing Excellence
Why Global Brands Trust PAG Pharmatech
Built to withstand the most demanding regulatory audits and international customs inspections, our operating model gives B2B buyers complete confidence from initial lab sample to full commercial release.
Compliance & Integrity
Full adherence to US FDA 21 CFR Part 111 (dietary supplements) and Part 117 (preventive controls). Audited and certified by SGS for SQF Edition 9 standards.
Scientific R&D Expertise
In-house formulation scientists, master blenders, and analytical chemists dedicated to ingredient stability, bioavailability enhancement, and clean-label design.
Export Ready
Complete documentation provided for global registration, including Certificate of Free Sale (CFS), Certificate of Analysis (CoA), Allergen Declarations, and BSE/TSE statements.
Dedicated Technical Support
Direct communication with experienced technical account directors. No communication lag, full transparency, and structured 90-day project tracking.
Springville, Utah Facility
State-of-the-Art Nutraceutical Infrastructure
Our 50,000+ sq. ft. cleanroom facility houses advanced blending, encapsulation, tableting, gummy depositing, stick-pack sachet filling, and automated packaging lines.
cGMP Cleanrooms
Automated Lines
Climate Warehousing
Analytical QC Lab
Encapsulation Suite100%
In-process quality testing from raw material verification to final container sealing.
Get Catalog Tri-Continental System
Integrated Global CDMO Capabilities
Our global infrastructure links US manufacturing with European regulatory compliance and Asian raw material procurement networks, protecting brand supply chains against single-point market disruptions.
USA · Utah Headquarters
Primary commercial hub providing FDA-registered, cGMP, and SQF Edition 9 manufacturing. Fast 8–12 week lead times for North American and global export orders.
Primary Manufacturing HubEU · Netherlands Plant
Fully certified EU-GMP operation delivering EFSA-aligned formulations, Novel Food compliance, and European market distribution support.
European Expansion HubAsia · Shenzhen Hub
Operational in 2026 for high-capacity batch manufacturing, raw material global sourcing leverage, and advanced extraction R&D.
Sourcing & Scale HubPartner with an FDA-Registered US CDMO
Request our complete product catalog, MOQ breakdowns, and facility audit documentation. Our technical directors respond within 24 business hours.
FDA registration does not constitute FDA approval or endorsement of any product. Certifications are held by our FDA-registered manufacturing operation; official documentation copies are available under NDA during supplier qualification.