98 John St, New Britain, CT 06051
Partner FAQ

Answers for prospective partners

Common questions from brands considering us as a development and manufacturing partner. Don’t see yours? Get in touch.

Do you offer formulation, or only manufacturing?

Both. Our Research division can develop a custom Ayurvedic-based formulation from concept, and our Manufacturing division produces it. You can also bring an existing, finished formula and we’ll manufacture it — or start with one of our established base formulations.

What’s the difference between custom, private label, and white label?

Custom means we develop a formulation specifically for you. Private label puts your brand on a product we help tailor. White label lets you bring an established base formulation to market under your own brand, quickly. We support all three.

What product formats can you produce?

We formulate the same standardized botanicals across capsules and tablets, powders and blends, effervescents, liquid tinctures, stick packs, functional beverages, and bulk or custom formats.

What are your minimum order quantities (MOQs)?

MOQs vary by product format, ingredient sourcing, and packaging. As a general guide, typical minimums start around 1,000–2,500 units for capsules and tablets, 1,000 units for powders and stick packs, and 500–1,000 units for liquids and tinctures, with bulk and custom runs quoted individually. Because we run everything from pilot batches to full commercial production, we can often start small and scale with you. Share your target volume on our Get Started form and we’ll confirm the exact MOQ for your project.

What are typical lead times?

Lead time depends on scope — a white-label run moves faster than a fully custom formulation that requires development and stability work. After reviewing your request, we provide a project-specific timeline from kickoff to finished, shipment-ready goods.

Are you GMP compliant? What quality standards do you follow?

Yes — production runs under GMP-compliant procedures with full batch records and traceability. We verify botanical identity, screen for heavy metals and microbials, and assay marker compounds, with stability studies supporting each product’s shelf life.

Do you provide Certificates of Analysis and third-party testing?

Yes. Certificates of Analysis (COAs) and third-party laboratory testing are available for every batch, so you have independent documentation of identity, purity, and potency.

How do you protect our formula and confidential information?

We treat partner formulas and information as confidential and are glad to work under a mutual non-disclosure agreement (NDA) before sharing project details. Your intellectual property remains yours.

Can you handle packaging, labeling, and fulfillment?

Yes. Beyond production we offer bottling, labeling, kitting, and shipment-ready packaging to your specification, so you receive finished goods rather than bulk product.

Do you offer samples or pilot batches?

Yes. Most projects begin with a small pilot batch to confirm the process and quality before we validate and scale to a full commercial run.

Do you support regulatory and label compliance?

We help partners navigate quality documentation and labeling considerations for dietary supplements. This is practical guidance from our experience, not legal advice — you remain responsible for final regulatory compliance, and we’re happy to coordinate with your regulatory counsel.

How do we get started?

Tell us about your product on our Get Started page — product type, format, target volume, and timeline. We’ll review it and follow up to scope your project.

Ready to start a project?

Send us the details and our team will follow up to scope development and production.

Get Started