Capsules, tablets, and powders are most common, with packaging options that include bottles, tubs & jars, and pouches (e.g., stick packs, sachets, gusseted pouches). Some projects also include liquids depending on scope and regulatory fit.

Both. We can develop a custom formula from your brief or provide ready-to-brand options that can be modified to your specification.

For true custom development, you retain ownership of your formula once the project is completed and any development fees are settled. We maintain technical files for manufacturing and quality records only.

Yes—within regulatory and IP boundaries. We analyze label disclosures and use R&D best practices to create a functionally comparable formula.

Manufacturing follows cGMP for dietary supplements with documented SOPs and batch records. Additional certification pathways (e.g., Organic, Kosher, Halal) may be supported depending on the project.

Yes. A finished-product CoA is issued per lot, reflecting the agreed specification and test results.

Yes. We review Supplement Facts, ingredient statements, and structure/function claims for U.S. dietary supplement regulations, and can flag items that may require legal or regulatory counsel.

MOQs vary by dosage form, packaging, and ingredient constraints. We’ll discuss practical starting volumes during scoping so the project is efficient and repeatable.

Yes. Pilot or small-batch runs are available to de-risk scale-up, validate process parameters, and generate market test inventory.

We support bottles, tubs & jars, and pouches (including stick packs, sachets, and gusseted pouches) plus retail cartons and compliant case-packing per routing guides.

Share your brief: target consumer, desired benefits/claims, dosage form, flavor (if applicable), certifications, volumes, and launch window. We’ll propose a scope covering formulation, testing, packaging, and production.