Contract Manufacturing RFQ Checklist for US Supplement Brands
What to lock in writing before you award a private-label or custom-formula run — unit MOQs, sample timelines, cGMP documentation, and East Coast logistics.
What MOQ should I expect for Zenith contract manufacturing?
Zenith’s published programme starts at 3,000 units for capsules, tablets and tinctures (liquids), and 500 kg for bulk powder blends. Confirm the exact dose form on the quote before you lock a launch date.
How long do samples and production runs take?
First bench sample is typically 10–15 working days from a written brief. A production run is typically 4–6 weeks from artwork approval. Get both milestones in writing on the RFQ.
What documents should a CM RFQ require?
Lot-specific COA, SDS, specification sheet, stability data where claimed, and clear lot traceability — plus allergen/GMO statements aligned to your label claims. A catalogue PDF is not a COA.
Why does ingredient stock location matter for a Long Island fill?
Production calendars slip when actives or empty capsules are “US stock” without a city. Zenith holds ingredients and packaging in Ronkonkoma, Long Island, New York, so the same technical conversation can cover both the fill and the critical inputs.