Who We Are
Ontario, California production campus — FDA Food Facility Registration on file, six dosage lines, published MOQs, and a typical sample-to-shelf path of about 11 weeks for on-plan launches.
HiGO Biotech Group is a U.S.-based OEM/ODM supplement partner. We coordinate formulation, private-label programs, and commercial production through FDA-registered, cGMP-certified manufacturing in Ontario, California — so brands can move from brief to shelf with one accountable team.
Every formula is grounded in evidence and reviewed by our R&D team before it touches a production line.
U.S.-based production with a worldwide supply chain — so your product is built to sell anywhere.
FDA registration No. 13565746238 is published through Dec 31, 2026. cGMP, HACCP, and California registration scans are on the credentials page — with clear status when the active renewal pack is the source for your audit. Production certificates list the Milliken Ave facility that releases your lots.
Six dosage formats under one roof, with the equipment, discipline, and formulation expertise to match.
Oils, lipid actives, precise dosing — booked in softgel campaign windows; schedule large POs early.
Fast-absorbing, age-flexible dosing.
High-dose actives at low cost-per-serving.
Taste-masking, gelatin or vegetarian shells.
Stick packs or tubs, instantised and flavoured.
Multi-format bundles for regimens.
Anonymised examples of how brands use HiGO for ODM, white-label, and scale-up — timelines and volume bands tied to our published MOQs and line capacity. Named client stories appear only with written permission.
Sports Nutrition
Benefit brief → first production pack-out in ~11 weeks
ODM pre-workout powder (caffeine + citrulline + electrolytes) filled into stick packs with subscription cartons — built for a first DTC launch.
Volumes and weeks vary with artwork freezes, raw-material lead times, and line scheduling.
Beauty from Within
White-label capsule SKU with retailer-ready documentation
Collagen peptide capsules with optional grape seed / HA support — branded bottles plus COA and batch records for marketplace onboarding.
Claim language and listing clearance remain the brand’s responsibility for each market.
Children's Nutrition
Fish-free omega softgel scheduled into softgel campaign windows
Vegetarian algae-oil softgel at ~100 mg DHA per softgel — flavour-masked options for kids’ nutrition positioning.
Confirm open softgel slots early — campaign calendars fill by season.
Digestive Health
Pilot mix → steady stick-pack replenishment
Multi-fiber powder in ~3 g stick packs — from 1,000 kg pilot mix to recurring strip-pack release for subscription brands.
Steady monthly volume depends on forecast, film lead times, and mix complexity.
Everyday Wellness
Familiar daily SKU from coating trial to bottle pack-out
Chewable Vitamin C (example 500 mg/tablet) — private-label path with flavour/coating options and bottle counts suited for retail.
Coating and flavour cycles are usually the pacing item before artwork freeze.
Family Wellness
Calibrated dropper bottles for DTC and export-minded brands
Vitamin D3 in MCT oil with calibrated dropper dosing — stability work and amber glass options for family wellness SKUs.
Serving strength and dropper calibration are confirmed at sample stage for each market.
Every HiGO engagement is staffed by four dedicated functions — formulation, quality, production, and client partnerships — so your formula, documentation, and timeline stay coordinated under one accountable team.
From brief to stable formula
Our formulation lab turns benefit briefs and existing formulas into production-ready specs — handling oxidation control, suspension stability, flavour masking, and accelerated shelf-life work across all six dosage formats.
cGMP discipline, every batch
Owns raw-material COA verification, in-process checks, finished-goods testing, and batch release — producing the documentation pack (COA, batch records) that clears retailer and marketplace onboarding without chargebacks.
Six dedicated dosage lines
Runs the softgel, tablet, capsule, liquid, powder, and daily-pack lines — each staffed and validated for its format, scaling from pilot runs to full-volume production on the same equipment.
Quote to first PO, coordinated
Your single point of contact from first inquiry through sample approval and first production run — quote response within 24 hours, pilot planning, and timeline coordination so launches stay on schedule.
A look at the equipment and lines that turn your formula into finished, shelf-ready product.
Separate softgel, tablet, capsule, liquid, powder, and pack lines — each staffed and validated for its format.
In-process and finished-goods testing on-site, with third-party ISO 17025 lab verification before release.
HiGO Biotech Group coordinates commercial projects from Ontario, California. Production runs through our FDA-registered, cGMP-certified Ontario manufacturing campus, serving brand partners across North America, Asia, and Europe.
This is a common and important question in contract manufacturing. HiGO Biotech Group coordinates your commercial project — formulation, private-label program, packaging, and delivery. Production itself runs through a registered Ontario manufacturing entity (SED Pharma Inc DBA Innova Nutra, 1500 S Milliken Ave), which holds the FDA facility registration and cGMP certification. This split between a commercial brand owner and a registered production entity is standard practice in U.S. supplement manufacturing. What matters for your launch is that every batch ships with the same documentation pack — COA, batch records, and release certificates — that retailers and marketplaces require for onboarding, all under the registered entity that produced your lots.
Six major formats: softgels, liquid drops, tablets, capsules, powder, and daily supplement packs — all under one roof. Softgel runs are scheduled in campaign windows; large softgel POs should be reserved early.
Yes. Our R&D lab handles everything from adapting an existing formula (OEM) to developing one from scratch (ODM), including stability and bioavailability work.
MOQ depends on format: capsules and tablets from 200,000 units; powder from 1,000 kg; softgels typically 300,000–500,000 units as capacity scales; liquid drops from about 50,000 bottles; daily packs from about 20,000 multi-packs. Share your target in the quote wizard for a precise figure.
On-plan projects typically: quote within 24 hours, representative samples in 2–3 weeks after formula sign-off, then pilot approval and first PO. Many launches reach shelf-ready status in about 11 weeks when artwork and materials stay on schedule.
Production is FDA-registered and cGMP-certified, with HACCP and California processed-food registration among other credentials. See our certifications page for numbers and downloadable documents.
Tell us about your project — format, volume, timeline — and we'll come back within 24 hours with a tailored quote.
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