Your Formula. Our Facility. Market-Ready in 30-40 Days.
You Have the Formula. We Handle the Rest.
Bring your formula to Makin, and we take it from there: raw material sourcing, manufacturing, quality testing, packaging, and dispatch. All from a single WHO-GMP certified facility in Pithampur, Madhya Pradesh.
Whether you call it third-party manufacturing, contract manufacturing, or toll manufacturing, the principle is the same: your formula, our facility, our quality systems.
We serve brands manufacturing for India and those supplying international markets, with the certifications and documentation to support both.
Two Ways We Work With You
You Have a Ready Formula
You Bring:
- Finished formula specification
- Ingredient and raw material specifications
- Artwork and packaging requirements
- Target market and regulatory requirements
We Handle:
- Raw material sourcing and qualification
- WHO-GMP manufacturing
- Full quality testing and batch release
- Primary and secondary packaging
- Certificate of Analysis and batch documentation
Your Formula Needs Some Development Support
You Bring:
- Product concept and target health area
- Partial formula or reference product
- Dosage form and market requirements
We Handle:
- Formula review and finalisation
- Optimisation for manufacturing scale
- Prototype development and specification confirmation
- Full commercial manufacturing once approved
How a CMO Order Works at Makin
Five steps from brief to finished product
Submit Your Brief
Share your formula, dosage form, target market, and packaging requirements. We confirm feasibility within one business day.
Material Review and Sourcing
We review your formula and source all raw materials from our qualified supplier network. Client-supplied materials accepted on request.
Artwork Approval
Our in-house design team prepares your packaging artwork. Production begins after your sign-off. The 30-40 day clock starts here.
Manufacturing and Testing
Your product is manufactured under WHO-GMP conditions with full in-process and finished product quality testing.
Batch Release and Dispatch
The finished product is dispatched with a Certificate of Analysis, batch records, and all export documentation required for your market.
What We Can Manufacture for You
We manufacture across 15+ dosage forms from tablets, softgels, and capsules to syrups, creams, topicals, and aerosols. For the full list of dosage forms, packaging formats, and production capacity figures, visit our CDMO Services page.
The Same Standards. Every Batch.
Third-party orders at Makin carry the same quality obligations as every other product that leaves our facility WHO-GMP manufacturing, in-house QC testing, and full batch documentation as standard.
Every Batch Includes
Certificate of Analysis
GMP Certificate copy on request
Manufacturing license
Manufacturing for India and International Markets
India Domestic
- FSSAI-compliant manufacturing
- AYUSH GMP certified
- Ayurvedic, Siddha and Unani Drugs Licences
- Full domestic regulatory documentation
Export Markets
- USFDA registered - US market
- WHO-GMP - globally accepted
- TBS GMP - East Africa
- HALAL certified - Middle East and Muslim-majority markets
Ready to Start Your Manufacturing Order?
Tell us your dosage form, target market, and approximate monthly volume. We will respond within one business day with a feasibility confirmation and quote outline without obligation.
All volume requirements are discussed during the initial brief. We work with established brands and businesses, helping them place their first manufacturing order.