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.

HiGO manufacturing equipment

Our advantages

Why brands choose HiGO to manufacture their supplements.

One roof, six formats

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

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

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

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.

1

Raw material inspection

Incoming actives and excipients verified against COA before release.

2

Formulation preparation

Blend/fill prepared and standardised to your active-content spec.

3

Production

Format-specific manufacturing under controlled conditions, with in-process QC.

4

Visual inspection

Optical and manual sorting removes any out-of-spec units.

5

Packaging

Bottling, blistering, or sachet packing with your label and artwork.

6

Final QA & release

Finished-goods testing, documentation review, and batch release.

From raw material to release

cGMP discipline across inspection, production, packaging, and final QA — so every batch ships with documentation your brand can stand behind.

FDA Registered FacilityFDA Registered Facility
cGMP Certified FacilitycGMP Certified Facility
Non-GMO Advanced FormulaNon-GMO Advanced Formula
Lab TestedLab Tested
Made in USAMade in USA

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