Direct Manufacturing Transparency
Essential Information for Global Purchasing Partners
Whether you are scaling an established international sports nutrition label or creating a clinical wellness product, find complete details about our US-based manufacturing processes below.
Production & Minimum Order Quantities (MOQs)
Our minimum order quantities are designed to support both emerging brands and enterprise distributors:
- Private Label Supplements: Starts at 300 units for stock, laboratory-tested formulas.
- Custom Powder Formulations: Starts at 500 tubs or pouches.
- Custom Encapsulation & Tablets: Starts at 1,000 bottles.
Low entry thresholds allow international buyers to validate new regional markets without over-committing working capital.
Standard lead times typically range between 4 to 6 weeks once raw material identity testing is complete, label artwork is approved, and packaging components are on site.
Custom formulations requiring novel raw material sourcing or specialized flavor development may require 8 to 12 weeks. Your dedicated account manager provides weekly milestone tracking from raw material staging to final QA batch release.
Nutracap is a direct contract manufacturer operating a state-of-the-art production plant in Norcross, Georgia, USA. We handle raw material procurement, precision blending, encapsulation, bottle filling, induction sealing, labeling, and quality testing under one roof. You deal directly with our facility—eliminating broker markups and communication bottlenecks.
Quality Assurance & Regulatory Compliance
Yes. Nutracap operates under full compliance with US FDA 21 CFR Part 111 dietary supplement cGMP guidelines. Our facility undergoes regular internal audits, third-party inspections, and quality verification. Every master manufacturing record (MMR) is fully documented to guarantee lot-to-lot consistency and total traceability.
Quality and safety are built into every stage of production:
- Incoming Raw Material Testing: FTIR identity testing, assay verification, and microbiological screening on every incoming lot.
- In-Process Quality Checks: Weight uniformity, tablet hardness, friability, disintegration testing, and blend uniformity.
- Finished Goods Analysis: Potency confirmation, microbiological screening, and heavy metal analysis (Lead, Arsenic, Cadmium, Mercury) via accredited third-party laboratories.
Yes. We produce formulations tailored for strict global market requirements, including Halal certified production runs, vegetarian/vegan HPMC capsules, non-GMO blends, allergen-free setups, and gluten-free compliance documentation.
International Shipping & Export Support
We routinely support international importers and distributors across Europe, the Middle East, Asia-Pacific, Africa, and Latin America. We supply comprehensive export dossiers, including:
- Certificate of Analysis (COA) for every finished batch
- Certificate of Free Sale (CFS)
- cGMP Manufacturing Declaration
- Detailed Product Master Specifications & Ingredient Allergen Statements
You maintain 100% ownership of your proprietary formulations. Nutracap operates under strict Non-Disclosure Agreements (NDAs) prior to formula review, guaranteeing that your proprietary blends, ingredient ratios, and flavor profiles remain confidential trade secrets.
Absolutly. We encourage prospective brand owners, qualified purchasing agents, and quality control auditors to inspect our cleanrooms, blending suites, high-speed encapsulation lines, and packaging bays. Facility tours are conducted by appointment.
20+ Years Expertise
Over two decades of proven experience formulating and scaling winning nutraceutical products worldwide.
100% Made in USA
Manufactured inside our FDA-registered facility in Norcross, Georgia with complete raw material traceability.
Dedicated Account Manager
One dedicated specialist coordinates formulation, artwork compliance, QA testing, and international freight.