Direct Access to US Technical & Sourcing Experts
PAG Pharmatech America LLC operates an FDA-registered manufacturing plant in Springville, Utah. We assist global brands, Amazon marketplace sellers, and international importers with end-to-end dietary supplement contract development and manufacturing (CDMO).
Custom Formulation & Technical Consultation
Our experienced R&D scientists evaluate your bill of materials (BOM), active ingredient potency target, and bioavailability goals. We support custom formulation, flavor matching, and stability optimization across gummies, tablets, powders, softgels, hard capsules, and pet nutrition.
Rigorous cGMP & Quality Release Standards
Every batch produced in our Springville facility undergoes rigorous in-house and third-party laboratory verification. Production strictly adheres to 21 CFR Part 111 (Dietary Supplements) and 21 CFR Part 117 (Preventive Controls for Human Food) regulations.
We provide a comprehensive documentation package with each completed batch release, including Certificate of Analysis (COA) for identity, potency, heavy metals, and microbiological safety, along with full batch production records.
Global Export & International Logistics
For international buyers entering the US market or sourcing US-made products for export to Europe, Canada, Asia, or the Middle East, our regulatory experts issue clean export certificates, certificate of free sale, and full product specifications tailored to destination market requirements.
2322 W 500 N Suite P
Springville, UT 84663, USA
+1 (385) 521-6376
Monday – Friday: 9:00am – 6:00pm (Mountain Time)
Saturday – Sunday: Closed
| Dosage Form | Minimum Volume |
|---|---|
| Gummies (Pectin / Gelatin) | 6,000 Bottles / Jars |
| Hard Capsules (HPMC / Bovine) | 5,000 Units |
| Softgels (Omega-3 / Oils) | 5,000 Units |
| Tablets (Chewable / Film Coated) | 5,000 Units |
| Powders & Stick Packs | 300 kg Bulk / Blends |
| Pet Soft Chews & Nutrition | 300 kg or 2,000 Units |
Common Sourcing Questions
Standard private label orders ship within 8 to 10 weeks. Fully custom formulations requiring novel flavoring, custom mold creation, or complex active ingredient sourcing take 12 to 16 weeks, including pilot run verification and analytical stability screening.
Yes. We strictly respect intellectual property. A formal mutual non-disclosure agreement (NDA) can be executed before sharing full formula specifications, proprietary ingredient stacks, or custom packaging designs.
Our facility holds FDA facility registration, cGMP compliance under 21 CFR 111 & 117, and SQF Edition 9 certification. Depending on ingredient qualification, product runs can also be certified Halal, Kosher, or USDA Organic.
Start Your Dietary Supplement Production Project
Connect with our Utah-based technical representatives to discuss your formulation, batch volume, and launch schedule.
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