Facility Location
Enova Science, LLC
4740 South Cleveland Ave.
Fort Myers, FL 33907, United States
70,000 sq. ft. NSF GMP Certified Plant
NSF GMP · FDA Registered · Made in USA
Contact Us – Request a Manufacturing Quote
Partner directly with our Florida-based formulation specialists, R&D scientists, and export logistics team for turnkey OEM/ODM supplement manufacturing.
Direct B2B Communication
Connect With Our USA Production Facility
We provide overseas brand owners, health supplement importers, and global distributors with direct access to technical formulation, regulatory guidance, and commercial manufacturing quotes.
Sales & R&D Team
Consult with technical engineers regarding ingredient decks, capsule sizing, gummy pectin bases, powder blend flowability, and private label stock formulas.
Quotes returned in 48 hours
Global Supply Support
Full support for export documentation, Amazon Seller Central COA verification, Halal/Kosher sourcing, and global freight containerization.
Worldwide freight dispatch
Enterprise Procurement
Turnkey Contract Manufacturing Parameters
From initial feasibility analysis to raw material verification, pilot trial batches, and final cGMP batch release, our operational standards back every procurement project.
Custom Formula & Private Label MOQ Tiers
We accommodate emerging nutraceutical brands and established international distribution networks through structured minimum order tiers:
- Private Label Stock Formulas: Starting from 5,000 finished units
- Custom Capsule & Tablet Runs: Scalable from 10,000 units
- Custom Gummy Production: Pectin and gelatin formats from 10,000 bottles
- Bulk Powders & Stick Packs: Blending runs up to 5,000+ kg per batch
Quality Assurance & Regulatory Documentation
Every shipment is backed by comprehensive analytical testing conducted in accordance with 21 CFR Part 111 cGMP standards:
- Finished Product Certificate of Analysis (CoA) with every lot
- Raw material identity, potency, and heavy metal screening
- Microbial safety validation & stability testing options
- Amazon compliance dossiers & international import documents
Export Standard
Streamlined B2B Onboarding Workflow
How our contract manufacturing team assists overseas procurement buyers through technical evaluation and production execution.
- 01
RFQ Evaluation
Submit your active ingredient deck, target dosage form, serving sizes, bottle specs, and estimated annual volume requirements.
- 02
R&D Feasibility
In-house chemists evaluate active overages, excipients, flow properties, flavor systems, and regulatory ingredient boundaries.
- 03
Trial Sampling
Physical pilot samples (gummies, capsules, flavored powders) are engineered and shipped to your location for sensory evaluation.
- 04
cGMP Production
Raw materials undergo quarantine verification; blending, encapsulation, tableting, or depositing runs in independent HVAC clean rooms.
- 05
Quality Release
Finished goods are tested, audited by Quality Assurance, cleared with executed batch records, and prepared for export shipment.
B2B Purchasing Guidance
Frequently Asked Procurement Questions
Clear guidelines for international buyers evaluating contract supplement manufacturers in the USA.
To provide a detailed formal quotation, our sales engineers need your desired dosage form (capsule, gummy, powder, tablet, or liquid), target active ingredients with dosages, packaging requirements (bottle count, blister pack, or stick pack), and initial production quantity.
Once formula parameters and active specifications are agreed upon, initial R&D pilot samples are generally produced and dispatched within 5 to 7 working days, allowing your team to evaluate flavor, color, texture, and capsule size.
Every batch includes a finished product Certificate of Analysis (CoA), Certificate of Free Sale (where applicable), cGMP Compliance Statement, complete ingredient breakdown, allergen statements, and batch lot tracking records.
Yes. In addition to custom OEM formulas, we maintain an extensive catalog of pre-formulated stock products (capsules, gummies, powders) available for white label branding, significantly reducing time-to-market for international launch schedules.
Start Your Contract Manufacturing Inquiry Today
Speak directly with our technical team to discuss formula feasibility, request pricing tiers, or review regulatory compliance requirements for your dietary supplement brand.