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Contract Manufacturing

End‑to‑end private‑label and custom formulation for herbal supplements & better‑for‑you foods—GMP aligned, documentation‑first, with live project visibility.

GMPISOFSSAIHACCPFDA reg. (where applicable)

Capabilities

From white‑label to full custom NPD—formats, packaging and compliance tailored to your market.

Dosage Forms

  • Capsules & Tablets (veg/gel; coated)
  • Powders & Drink mixes
  • Gummies (pouches / bottles)
  • Teas & Infusions

Packaging & Labelling

  • Bottles, jars, blisters, sachets, pouches
  • Retail & club packs; ship‑ready cartons
  • Artwork support & label compliance
  • Barcodes, batch & trace printing

Testing & Documentation

  • COA, Microbial, Heavy metals, Pesticides
  • Stability studies (as applicable)
  • Allergen & GMO‑free declarations
  • Traceability dossiers

Our Process

  1. Scope & brief: target market, claims, pack sizes, volumes
  2. Formulation & prototypes: samples + initial stability/organoleptic checks
  3. Artwork & compliance: label review for destination market
  4. Pilot → Scale: production, QC testing, documentation bundle
  5. Dispatch & live tracking; post‑shipment support

Quality & Compliance

We operate with a documentation‑first approach so approvals are faster and repeatable.

COA per batch Microbial & Heavy metals Pesticides (on request) Allergen & GMO‑free Stability summary (as applicable) Specs & MSDS HS code & Origin Traceability mapping

MOQs & Timelines

Typical MOQs

  • Capsules/Tablets: 5k–20k units
  • Powders: 200–500 kg
  • Gummies: 10k–50k units
  • Private‑label variants on request

Lead Times

  • White‑label: 3–5 weeks
  • Custom formulation: 6–10 weeks
  • Reorders: 2–4 weeks (spec‑dependent)

Commercials

  • Quoted per spec & pack configuration
  • Samples offset on PO (where applicable)
  • Payment terms based on project

Project Visibility & Integrations

Keep your team and systems in sync during development and production.

Project Portal

  • Milestones, sample sign‑offs, docs in one place
  • Versioned artwork & spec handoffs
  • Live production & dispatch updates

CSV / REST Hooks

  • PO, ASN & Invoice sync (CSV schedules)
  • REST webhooks for milestones & doc links
  • Slack/Email notifications (optional)

FAQs

Can you develop a new formulation from a brief?

Yes. Share intended claims, actives, target market and price points. We propose a formula, samples and test plan.

Do you support label design and compliance?

We provide artwork guidance and compliance checks for destination markets. Final regulatory sign‑off remains with the buyer.

Can we start with small batches?

Pilot runs are available for select formats. We’ll advise the most economical MOQ for your case.

What testing is included?

COA per batch (identity, purity) plus microbial and heavy metals. Additional panels (pesticides, stability) on request.