Large-Scale Production Capacity
70,000 sq. ft. facility with 5,000+ kg blending capability and dedicated rooms that keep sensitive botanical, probiotic and allergen formulas separated.
NSF
NSF GMP Registered
cGMP Compliant
FDA Registered
Made in USAUSDAORGANIC
Organic Ingredient Support
Halal & Kosher Options Why Brands Choose Enova
A Single U.S. Partner From Formula Brief to Palletized Product
Nearly two decades of nutraceutical production experience, 17 independent production rooms and in-house R&D, quality control and packaging — so your brand deals with one accountable manufacturer instead of four vendors.
Full Custom Formulation
Our R&D chemists evaluate potency overages, excipient compatibility, flowability, flavor masking and stability before a single production batch is scheduled.
Documented Compliance
Batch records, Certificates of Analysis, GMP certificates, allergen statements and label-claim support built into every project — not requested afterwards.
Predictable Lead Times
Quotes in about 48 hours, R&D pilot samples in roughly 5 working days and standard turnkey production in approximately 8 weeks after final approval.
Our Facility
Take a Virtual Tour of Our cGMP Manufacturing Plant
See how raw materials are received, verified, blended, encapsulated, deposited, filled and packaged inside our Fort Myers, Florida facility.
Formulating custom gummy samples in our in-house R&D lab
70,000Square feet of NSF GMP registered production space in Fort Myers, Florida
17Independent production rooms for cross-contamination control
20 yrsOf nutraceutical manufacturing, blending and packaging experience
Every Form. Every Formula.
Custom Supplement Manufacturing Capabilities
From high-potency capsules to pectin gummies and single-serve stick packs, each dosage form is produced, tested and packaged under one documented quality system.
Capsule Supplement Manufacturing
Vegetarian HPMC and gelatin capsules from size 000 to 3, with precise fill weights, botanical extracts, oils and multi-ingredient blends.
Capsule capabilities
Gummy Supplement Manufacturing
Pectin or gelatin bases, sugar-free options, custom shapes, colors and flavors with verified actives after heat and depositing.
Gummy formulas
Powder Supplement Manufacturing
Protein, collagen, greens, electrolyte and superfood blends with 5,000+ kg batch blending, flavor systems and excellent mixability.
Powder formulas
Tablet Supplement Manufacturing
Compressed, bi-layer and coated tablets with controlled hardness, disintegration profiles, custom tooling and debossing.
Tablet formulas
Liquid Supplement Manufacturing
Tinctures, dropper bottles, liquid shots and functional beverages with preservative systems validated for shelf-life stability.
Liquid formulas
Stick Pack & Sachet Manufacturing
Single-serve stick packs and sachets for travel-friendly powders, hydration mixes and probiotic formulas with precise dose filling.
Stick pack formats
Probiotic, Prebiotic & Postbiotic Formulas
Spore-forming strains, heat-stable postbiotics, digestive enzymes and fiber blends with CFU overage planning and low-humidity handling.
Biotic capabilities
Cosmetic & Nutricosmetic Manufacturing
Beauty-from-within capsules, powders and topical companion products for collagen, skin, hair and nail positioning.
Cosmetic formulas
Pet Supplement Manufacturing
Companion-animal powders, liquids and chews for joint, digestive, skin and coat support — including private label pet wellness lines.
Private label options Private Label
Ready-to-Market Private Label Supplement Formulas
Skip formulation development. Select a proven stock formula, apply your branding and packaging, and move straight to production — typically from 5,000 units with volume tiers above.
Botanical Capsule Formula
Stress & balance positioning · 5,000 unit start
Antioxidant Capsule Formula
Healthy aging positioning · 5,000 unit start
Beauty Capsule Formula
Skin, hair & nails positioning · 5,000 unit start
Perilla & Enzyme Capsules
Digestive comfort positioning · 5,000 unit start
How It Works
From Formula Review to Finished, Released Product
A transparent five-stage workflow used on every project, so you always know what is approved, what is being tested and what is scheduled.
- 01
Requirements & Scope
Share actives, overages, label claims, serving size, servings per container and packaging targets. We review feasibility and scope the project.
- 02
Agreement & Specifications
Formula, packaging, testing scope, documentation deliverables and production volumes are locked into a written manufacturing agreement.
- 03
R&D & Pilot Samples
Our lab checks ingredient stability, capsule sizing, powder flow, flavor and texture, then produces pilot samples until you approve them.
- 04
Final Approval
Sign-off on potency, samples, artwork placement, packaging components and testing requirements before raw material procurement begins.
- 05
cGMP Production & Release
Production runs under documented cGMP controls; finished batches are tested, reviewed and released with full records and Certificates of Analysis.
Quality & Documentation
What We Test, Record and Deliver With Every Batch
Retail buyers, marketplaces and international importers all ask for evidence. This is the documentation package our quality team prepares as standard.
| Stage | Controls Performed | Deliverables You Receive |
|---|---|---|
| Raw material intake | Supplier qualification, identity verification, quarantine until released, allergen and origin review. | Ingredient specifications and supplier Certificates of Analysis on request. |
| In-process manufacturing | Blend uniformity checks, weight and fill verification, line clearance, metal and sieve controls. | Executed batch record summary tied to your lot number. |
| Finished product | Potency of label actives, microbial limits, heavy metals and organoleptic evaluation per specification. | Finished product Certificate of Analysis (CoA). |
| Packaging & labeling | Artwork proofing, label claim cross-check, seal integrity, lot and expiry coding. | Approved artwork proof plus packaging component specifications. |
| Release & retention | Quality review and release decision, retained samples stored for future reference. | GMP certificate, release documentation and marketplace-ready compliance files. |
Certifications & Options
- NSF GMP registered & cGMP compliant
- FDA registered facility
- USDA Organic ingredient support
- Halal sourcing & Kosher production options
Typical Timelines
- Quote response: about 48 hours
- R&D pilot samples: about 5 working days
- Turnkey production: about 8 weeks
- Repeat orders: shorter, formula already validated
Order Volumes
- Private label stock formulas from 5,000 units
- Custom formulas quoted by form & actives
- Volume tiers at 10k / 50k / 100k+ units
- Bulk powder and bulk capsule supply available
Common Queries
Frequently Asked Questions
Clear answers about capabilities, MOQs, R&D support, documentation and quality standards at Enova Science.
Yes. Our R&D team develops fully custom formulations from your ingredient deck, competitor benchmark or concept brief. We also offer ready-to-brand private label stock formulas, which reduce development work to labeling, packaging and compliance review only.
Private label stock formulas typically start at 5,000 units. Custom formulations are quoted based on dosage form, active ingredient cost, testing scope and packaging format, with improved pricing tiers at 10,000, 50,000 and 100,000+ units.
Quotes are generally returned within 48 hours, R&D pilot samples within about five working days, and standard turnkey production in approximately eight weeks after final sign-off. Raw material availability and packaging component lead times are the main variables.
Our 70,000 sq. ft. facility in Fort Myers, Florida is NSF GMP registered, cGMP compliant and FDA registered. We also support Made in USA production, USDA Organic ingredient sourcing, Halal ingredient options and Kosher production runs.
Every batch follows documented cGMP procedures: raw material identity verification, in-process blend and fill checks, and finished product testing for label-claim potency, microbial limits and heavy metals. Retained samples, executed batch records and Certificates of Analysis are maintained for traceability.
Yes. We provide Certificates of Analysis, GMP certificates, ingredient specifications, allergen and nutritional data, and the supporting documentation commonly requested by Amazon Seller Central, distributors and overseas importers.
We manufacture in the United States and support export shipments worldwide, coordinating with your freight forwarder on palletization, export documentation and destination-market labeling requirements.
Ready to Discuss Your Next Supplement Project?
Send us your dosage form, target formula and volume expectations. Our manufacturing team will review feasibility and respond with next steps, usually within two business days.