Global Buyer & Brand Focus
We provide international distributors and overseas dietary supplement brands with turnkey manufacturing, export compliance, customs clearance support, and Certificate of Analysis (CoA) release with every single lot.
NSF
NSF GMP Certified
cGMP Audit Passed
FDA Registered
100% Made in USAUSDAORGANIC
USDA Organic Certified
Halal Registered
Executive Overview
A Fully Integrated U.S. Dietary Supplement Contract Manufacturer
Enova Science, LLC is a premier, full-service nutraceutical contract manufacturer based in Fort Myers, Florida. Operating 17 independent production suites with full environmental controls, we specialize in high-potency capsules, gummies, powders, tablets, liquids, and stick packs for leading global brands.
17 Dedicated Production Suites
Our facility features independent cleanroom suites with separate air handling systems, preventing cross-contamination for sensitive botanical extracts, probiotics, and allergen-sensitive formulations.
100+ Years Combined R&D Expertise
Our formulation scientists and quality assurance chemists bring over a century of collective expertise in active ingredient overages, bioavailability enhancement, taste-masking, and stability testing.
70,000 Sq. Ft.
NSF GMP registered production space in Fort Myers, Florida
17 Cleanrooms
Isolated production suites for strict contamination control
5,000+ kg
Daily powder and liquid micro-blending capacity
1k – 100k+ Units
Scalable batch sizes for growing and enterprise brands
Our Journey & Operational Excellence
Engineered for Transparency, Speed, and Compliance
Built from the ground up to revolutionize nutraceutical manufacturing, Enova Science offers international clients an agile, reliable alternative to traditional contract manufacturers.
Our Start & Vision
Founded in 2009, Enova Science set out with a clear mission: offering first-to-market, scientifically validated nutritional formulations. Over nearly two decades, we have continuously optimized raw material sourcing, automated blending, and high-speed encapsulation lines to provide clients with a distinct competitive advantage in global marketplaces.
Industrial Scalability
Equipped with two pharmacy operations, high-speed capsule fillers, pectin gummy depositing lines, and automated stick pack fillers, our plant handles projects from 1,000 pilot runs to 100,000+ commercial units. In-house sensory panels evaluate product mouthfeel, aroma, and flavor before full-scale commercialization.
Turnkey R&D Execution
Our New Product Development (NPD) team guides global clients through ingredient compatibility, dose weight optimization, label claim validation, regulatory filing, and packaging design. Pre-market sensory panels deliver data-driven insights, ensuring optimal consumer acceptance and repeat purchase rates.
Inside Enova Science
Tour Our Fort Myers cGMP Production Facility
See our automated high-speed capsule, gummy, powder, and liquid lines operating under audited 21 CFR Part 111 cGMP compliance standards.
Automated encapsulation and R&D pilot lab at Enova Science plant, Fort Myers, Florida
Regulatory & Compliance Standards
Independently Audited & Certified Manufacturing Facility
We maintain real, verifiable third-party certifications to ensure your brand meets strict FDA, EU, and international health authority guidelines.
USDA Organic Certification
Audited compliance with National Organic Program (NOP) standards for handling, blending, and packaging 100% organic botanical and dietary powders.
NSF International cGMP
Certified under NSF/ANSI 173 Section 8 for dietary supplement facilities. Comprehensive third-party audits verify process control, sanitation, and safety.
Halal Facility Registration
Registered with the American Halal Foundation (AHF) for contract production of nutraceuticals adhering to international Halal dietary standards.
FDA Facility Registration
Fully registered with the U.S. Food & Drug Administration under FSMA & 21 CFR Part 111 cGMP regulations, supporting seamless international export.
Zero-Defect Commitment
Four-Stage Quality Control & Batch Release Protocol
Every order produced at Enova Science undergoes rigorous analytical, physical, and microbiological verification before entering shipment.
| Quality Phase | Testing & Inspection Protocols | Documentation Delivered |
|---|---|---|
| 1. Raw Intake Verification | 100% raw material quarantine, FT-IR raw identity testing, heavy metals screening (ICP-MS), and micro assay. | Raw Material Specification Sheets & Supplier CoA Verification. |
| 2. In-Process Suite Controls | Blend uniformity checks, individual dose weight consistency monitoring, sieve analysis, and line clearance audit. | Batch Master Record Executed Log with complete Lot Traceability. |
| 3. Finished Goods Assays | Third-party analytical testing for active potency claims, heavy metals, pesticides, pathogens, and disintegration rate. | Full Finished Product Certificate of Analysis (CoA). |
| 4. Final Release & Shipping | Quality Assurance team sign-off, packaging seal integrity verification, retained sample archival, export palletization. | GMP Certificate, Free Sale Certificate, Export Documentation & CoA Package. |
International Buyer FAQ
Frequently Asked Questions
Essential details on custom manufacturing, export paperwork, MOQs, packaging, and quality assurances for global brands.
Yes. Our in-house R&D chemists formulate custom products from scratch based on your targeted active ingredients and benefit claims. We also maintain a wide catalog of ready-to-market private label formulas for rapid brand launches.
Private label stock products start at 5,000 units. Custom formulations are quoted based on dosage format, active ingredient complexity, and packaging type, with volume pricing discounts at 10,000, 50,000, and 100,000+ units.
Total costs vary depending on active ingredient costs, dosage form (e.g., pectin gummies vs. standard capsules), volume, and custom packaging. We supply detailed, transparent line-item quotes within 48 hours covering R&D, manufacturing, testing, and packaging.
Yes. We manufacture in the USA and export globally. We coordinate with international freight forwarders and provide export documentation, including Certificates of Free Sale, cGMP Certificates, and Certificates of Analysis (CoA).
We offer automated packaging lines for HDPE/PET bottles, glass bottles, blister packs, single-serve powder stick packs, sachets, dropper bottles, and bulk powder/capsule drums.
Quotations are issued within 48 hours. R&D pilot samples take approximately 5 working days. Full turnkey production runs take around 8 weeks following final sign-off on formula and artwork.
Yes. We provide complete regulatory support for Amazon Seller Central compliance, including ISO 17025 accredited CoA testing, cGMP facility certificates, and label accuracy documentation.
Every batch undergoes strict cGMP controls: raw material identity testing, in-process fill/weight checks, and final third-party lab testing for potency, heavy metals, and microbes. Certificates of Analysis are generated for every production lot.
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