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Formulation partnerships start here

Submit your manufacturing specifications or franchise territory requests. Our dedicated corporate response team reviews and replies to all verified pharmaceutical inquiries within 24 hours.

Frequently asked questions

Review essential compliance, minimum order quantity, and regulatory documentation requirements for our WHO-GMP certified third-party manufacturing and PCD franchise partnerships.

What are the MOQs?

Are you WHO-GMP certified?

How do franchise rights work?

Our minimum order quantities vary by formulation. Generally, tablets require a minimum batch of 100,000 units, while liquid syrups require 10,000 bottles per run.

Yes, all manufacturing facilities are fully WHO-GMP compliant. We provide complete batch documentation, certificates of analysis, and regulatory support for license registration.

We grant exclusive monopoly franchise rights for designated regional territories. This ensures no other distributor can market our certified formulations within your agreed boundary.