All production activities at CDRI are conducted in strict accordance with international GMP standards and are optimized for scalability, consistency, and efficiency.

Site 1. Solid Dosage Forms

- Manufacturing of tablets and capsules
- Two independent production lines with Class D cleanroom environments

Site 2. Cytostatic Solid Dosage Forms

- Dedicated production site for oral anticancer medicines
- Class D cleanroom standards

Site 3. Sterile Injectable Products
- Hormonal injectables in ampoules and vials
- Class A cleanroom environment

Site 4. Packaging
- Primary and secondary packaging operations
- Automated blistering and vial filling lines
- Environmental control within Class D cleanroom zones