Free QuoteAbout Higo
Manufacturing process
The equipment, controls, and workflow used across HiGO's two U.S. manufacturing facilities — with facility-specific credentials confirmed by project.
Equipment & production capacity
Two U.S. manufacturing facilities supporting scalable production and documented quality across six dosage formats.
Dedicated format lines
Capabilities across softgel, tablet, capsule, liquid, powder, and pack formats, assigned by facility and project requirements.
On-site quality labs
In-process and finished-goods testing requirements are defined by project specification and the applicable facility quality program.
Scalable capacity
Published capacity includes up to 92,000 capsule bottles/day, 80,000 tablet bottles/day, and 120,000 sachets/day. Facility assignment is confirmed during project review.
cGMP documentation
Traceability, COA, batch-record, and release-document requirements are defined for the assigned facility and project.
Our advantages
Why brands choose HiGO to manufacture their supplements.
Two facilities, six supported formats
Softgels, tablets, capsules, liquids, powders, and daily packs are supported across the U.S. manufacturing network, with production location and applicable credentials confirmed by project.
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 and commercial-volume options are reviewed against format, facility, equipment, and qualification requirements before scheduling.
Two facilities, six formats
See the full nutraceutical manufacturing program — capabilities, dosage formats, and project-specific credential guidance.
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.
