About Higo
Manufacturing process
The equipment, advantages, and workflow behind every HiGO batch — cGMP from raw material to release.
Equipment & production capacity
A U.S.-based, FDA-registered facility built for scale and documented quality across every dosage format.
Dedicated format lines
Separate softgel, tablet, capsule, liquid, powder, and pack lines — each staffed and validated for its format.
On-site quality labs
In-process and finished-goods testing on-site, with third-party ISO 17025 lab verification before release.
Scalable capacity
Six dedicated lines — up to 92,000 capsule bottles/day, 80,000 tablet bottles/day, 120,000 sachets/day, and more across formats. Pilot runs scale to full volume on the same line.
cGMP documentation
Every batch ships with full traceability — COA, batch records, and release documentation.

Our advantages
Why brands choose HiGO to manufacture their supplements.

One roof, six formats
Softgels, tablets, capsules, liquids, powders, and daily packs — all manufactured in-house, so your multi-format range ships from one quality system.

R&D that de-risks launch
Our lab handles oxidation control, suspension stability, and bioavailability — catching formulation issues at pilot, not at scale.

cGMP discipline, every batch
Raw-material COA, in-process checks, and finished-goods testing against your spec — documented end-to-end, release on sign-off only.

Flexible MOQ, real scaling
Pilot runs for first-to-market validation, scaling seamlessly to full-volume production on the same line — no requalification mid-launch.
The production flow
Six stages, every one documented — from raw material to released finished goods.
Raw material inspection
Incoming actives and excipients verified against COA before release.
Formulation preparation
Blend/fill prepared and standardised to your active-content spec.
Production
Format-specific manufacturing under controlled conditions, with in-process QC.
Visual inspection
Optical and manual sorting removes any out-of-spec units.
Packaging
Bottling, blistering, or sachet packing with your label and artwork.
Final QA & release
Finished-goods testing, documentation review, and batch release.






