PAG Pharmatech America provides end-to-end contract formulation, manufacturing, primary packaging, and laboratory release testing under strict US FDA regulatory standards. Our Springville, Utah facility manufactures six distinct dosage forms tailored to DTC, retail, and international import compliance requirements.
MOQ: 6,000 Units Advanced starchless depositing for high-precision botanical, vitamin, and mineral gummy supplements. Formulated with citrus pectin or pharmaceutical-grade bovine gelatin, offering heat-stable and sugar-free options with validated active ingredient survival rates.
MOQ: 5,000 Units High-speed automatic capsule filling for dry powders, herbal extracts, and granular formulations. Available in Non-GMO HPMC vegetable shells or bovine gelatin across sizes 000, 00E, 00, 0, 1, and 2, including delayed-release acid-resistant options.
MOQ: 5,000 Units Rotary die encapsulation engineered for lipid-based nutrients, liposomal formulations, and lipophilic actives like Omega-3 marine oils, CoQ10, Vitamin D3/K2, and MCT oil blends. Featuring nitrogen-flushed fill lines to prevent oxidation.
MOQ: 5,000 Units Heavy-duty rotary tablet compression for dense multivitamin formulations, chewables, and effervescent delivery systems. Options include custom debossing, aqueous film coating, enteric barrier coating, and bi-layer time-release technologies.
MOQ: 300 kg High-shear dry blending and pneumatic filling for pre-workout sports nutrition, whey/plant protein isolate, hydration electrolytes, and collagen peptides. Packaged in bulk canisters, flexible pouches, or automated single-serve stick packs.
MOQ: 300 kg / 2k Units Specialized companion animal health supplements produced in cold-extruded soft chew formats, functional powders, and liquid oils. Formulated according to AAFCO guidelines with verified palatability testing for canine and feline formulations.
Compare key parameters for international procurement, minimum batch sizes, and regulatory compliance features across our US CDMO production lines.
| Dosage Format | Standard MOQ | Typical Lead Time | Active Density & Bioavailability | Shell / Base Options | Primary Quality Certifications |
|---|---|---|---|---|---|
| Gummies | 6,000 Bottles | 8–12 Weeks | Moderate (up to 500mg/unit) | Pectin (Vegan), Bovine Gelatin | FDA cGMP, SQF Ed. 9, Kosher |
| Hard Capsules | 5,000 Bottles | 8–10 Weeks | High (up to 1,000mg/unit) | HPMC Vegetable, Bovine Gelatin | FDA cGMP, SQF Ed. 9, Halal, Kosher |
| Softgels | 5,000 Bottles | 8–12 Weeks | Superior for Lipids & Oils | Bovine Gelatin, Tapioca Starch | FDA cGMP, SQF Ed. 9, Halal |
| Tablets | 5,000 Bottles | 8–10 Weeks | Highest (up to 1,500mg/unit) | Aqueous Film Coating, Enteric | FDA cGMP, SQF Ed. 9, Kosher |
| Powders & Stick Packs | 300 kg per SKU | 6–8 Weeks | Custom Per Serving (1g–30g) | Bulk Canister, Sachet, Foil Stick Pack | FDA cGMP, SQF Ed. 9, USDA Organic |
| Pet Soft Chews | 300 kg / 2,000 Jars | 8–10 Weeks | Tailored Palatability Dosage | Cold-Extruded Real Meat / Plant Base | FDA cGMP (21 CFR Part 507), AAFCO |
Every product batch manufactured by PAG Pharmatech undergoes stringent physical, chemical, and microbiological validation inside ISO-accredited testing facilities.
FTIR and HPLC verification of all raw material ingredients prior to dispensing and blending.
Validated active potency verification ensuring 100% label claim compliance through shelf-life.
ICP-MS heavy metal testing (Lead, Arsenic, Cadmium, Mercury) and complete micro screening.
Full batch record transparency, master manufacturing records, and CoA issued with every shipment.
Essential technical and logistical answers for international brands and purchasing managers.
PAG Pharmatech provides a complete export documentation package with every international batch. This includes a batch-specific Certificate of Analysis (CoA), Certificate of Free Sale (CFS), cGMP Compliance Certificate, Allergen Statement, Non-BSE/TSE Certificate, and full ingredient origin declarations required by customs authorities across Europe, Asia, Latin America, and the Middle East.
Custom R&D formulation work, active ingredient sourcing, organoleptic flavor optimization, and initial pilot lab samples are typically completed within 14 to 21 business days. Accelerated stability testing and pilot batch validation occur concurrently to keep overall launch timelines within 90 days.
Yes. Our facility supports certified organic handling (USDA Organic), Kosher Pareve, and Halal production runs. We offer HPMC vegetable capsule shells, citrus pectin gummy bases, tapioca softgel shells, and clean-label excipients for brands targeting specialized consumer demographics.
We provide full turnkey packaging options including HDPE/PET bottle bottling with induction seals, child-resistant closures, blister packaging, unit cartons, stick pack pouching, shrink banding, and master case display packing. All packaging lines feature automated vision inspection and lot/exp inkjet coding.
Connect with our Springville, Utah CDMO engineering team to request detailed specs, sample production, or target pricing for your brand's next SKU.
FDA registration does not constitute FDA approval or endorsement of any product. Certifications are held by our FDA-registered manufacturing operation; certificate copies are available under NDA during supplier qualification.
