ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯏꯟꯗꯁꯠꯔꯤꯒꯤꯗꯃꯛ ꯀꯔꯀꯨꯃꯤꯟ ꯑꯦꯛꯁꯠꯔꯦꯛꯇꯁꯤꯡ ꯀꯔꯀꯨꯃꯤꯟ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯐꯣꯔꯃꯨꯂꯦꯁꯅꯁꯤꯡꯒꯤꯗꯃꯛ ꯍꯥꯏ-ꯄꯨꯔꯤꯇꯤ ꯀꯔꯀꯨꯃꯤꯟ ꯑꯦꯛꯁꯠꯔꯦꯛꯇꯁꯤꯡ ꯑꯃꯁꯨꯡ ꯁ꯭ꯇꯦꯟꯗꯔꯗꯥꯏꯖꯗ ꯍꯜꯗꯤ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯑꯦꯄ꯭ꯂꯤꯀꯦꯁꯅꯁꯤꯡꯗꯥ ꯀꯔꯀꯨꯃꯤꯟ
ꯀꯔꯀꯨꯃꯤꯟꯒꯤ ꯋꯦꯜ-ꯗꯣꯛꯌꯨꯃꯦꯟꯇꯦꯗ ꯐꯥꯔꯃꯥꯀꯣꯂꯣꯖꯤꯀꯦꯜ ꯄ꯭ꯔꯣꯄꯔꯇꯤꯁꯤꯡ
ꯑꯦꯟꯇꯤ-ꯏꯟꯐ꯭ꯂꯦꯃꯦꯇꯔꯤ ꯑꯦꯛꯇꯤꯕꯤꯇꯤ
COX-2 ꯏꯟꯍꯤꯕꯤꯁꯟ ꯑꯃꯁꯨꯡ NF-κB ꯄꯥꯊꯋꯦꯒꯤꯗꯃꯛ ꯑꯦꯛꯁꯇꯦꯟꯁꯤꯕꯂꯤ ꯁ꯭ꯇꯗꯤ ꯇꯧꯔꯕꯥ
ꯑꯦꯟꯇꯤꯑꯣꯛꯁꯤꯗꯦꯟꯠ ꯄ꯭ꯔꯣꯄꯔꯇꯤꯁꯤꯡ
ꯄꯣꯇꯦꯟꯠ ꯐ꯭ꯔꯤ ꯔꯦꯗꯤꯀꯦꯜ ꯁ꯭ꯀꯦꯕꯦꯟꯖꯤꯡ ꯑꯃꯁꯨꯡ ꯃꯦꯇꯦꯜ ꯆꯦꯂꯦꯁꯟ ꯑꯦꯕꯤꯂꯤꯇꯤꯁꯤꯡ
ꯔꯤꯁꯔꯆ ꯏꯟꯇꯔꯦꯁ꯭ꯠ
ꯑꯣꯅꯀꯣꯂꯣꯖꯤ, ꯅꯤꯎꯔꯣꯂꯣꯖꯤ, ꯀꯥꯔꯗꯤꯌꯣꯂꯣꯖꯤꯗꯥ ꯑꯦꯛꯇꯤꯕ ꯛꯂꯤꯅꯤꯀꯦꯜ ꯔꯤꯁꯔꯆ
ꯀ꯭ꯕꯥꯂꯤꯇꯤ ꯑꯁꯧꯔꯦꯟꯁ ꯅꯣꯠ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ-ꯒ꯭ꯔꯦꯗ ꯃꯇꯦꯔꯤꯌꯦꯜꯁꯤꯡ ꯄꯨꯝꯅꯃꯛ ꯑꯦꯟꯍꯦꯟꯁꯗ ꯇꯦꯁ꯭ꯇꯤꯡ ꯇꯧꯔꯤ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯑꯦꯄ꯭ꯂꯤꯀꯦꯁꯅꯁꯤꯡ
ꯑꯩꯈꯣꯌꯒꯤ ꯀꯔꯀꯨꯃꯤꯟ ꯃꯈꯜ ꯃꯈꯜꯒꯤ ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯑꯦꯄ꯭ꯂꯤꯀꯦꯁꯅꯁꯤꯡꯗꯥ ꯁꯔꯕ ꯇꯧꯏ
ꯗ꯭ꯔꯒ ꯐꯣꯔꯃꯨꯂꯦꯁꯅꯁꯤꯡ
ꯇꯦꯕꯂꯦꯇꯁꯤꯡ ꯑꯃꯁꯨꯡ ꯀꯦꯞꯁꯨꯜꯁꯤꯡꯗꯥ ꯑꯦꯛꯇꯤꯕ ꯅꯠꯔꯒꯥ ꯑꯦꯗꯖꯪꯛꯠ ꯏꯟꯒ꯭ꯔꯤꯗꯤꯌꯦꯟꯠ ꯑꯣꯏꯅꯥ ꯀꯔꯀꯨꯃꯤꯟ
API ꯃꯦꯅꯨꯐꯦꯛꯆꯔꯤꯡ
ꯍꯥꯏ-ꯄꯨꯔꯤꯇꯤ ꯀꯔꯀꯨꯃꯤꯟ ꯑꯦꯛꯁꯠꯔꯦꯛꯠ (95%+) ꯑꯦꯛꯇꯤꯕ ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯏꯟꯒ꯭ꯔꯤꯗꯤꯌꯦꯟꯠ ꯑꯣꯏꯅꯥ
ꯛꯂꯤꯅꯤꯀꯦꯜ ꯔꯤꯁꯔꯆ
ꯛꯂꯤꯅꯤꯀꯦꯜ ꯇ꯭ꯔꯥꯏꯌꯦꯜꯁꯤꯡ ꯑꯃꯁꯨꯡ ꯐꯥꯔꯃꯥꯀꯣꯂꯣꯖꯤꯀꯦꯜ ꯁ꯭ꯇꯗꯤꯁꯤꯡꯒꯤꯗꯃꯛ ꯁ꯭ꯇꯦꯟꯗꯔꯗꯥꯏꯖꯗ ꯀꯔꯀꯨꯃꯤꯟ
ꯇꯣꯄꯤꯀꯦꯜ ꯄ꯭ꯔꯤꯄꯦꯔꯦꯁꯅꯁꯤꯡ
ꯗꯔꯃꯦꯇꯣꯂꯣꯖꯤꯀꯦꯜ ꯐꯣꯔꯃꯨꯂꯦꯁꯅꯁꯤꯡ ꯑꯃꯁꯨꯡ ꯋꯨꯟꯗ ꯍꯤꯂꯤꯡꯒꯤꯗꯃꯛ ꯀꯔꯀꯨꯃꯤꯟ
ꯕꯥꯏꯑꯣꯑꯦꯚꯦꯂꯦꯕꯤꯂꯤꯇꯤ ꯔꯤꯁꯔꯆ
ꯑꯦꯟꯍꯦꯟꯁꯗ ꯕꯥꯏꯑꯣꯑꯦꯚꯦꯂꯦꯕꯤꯂꯤꯇꯤ ꯐꯣꯔꯃꯨꯂꯦꯁꯅꯁꯤꯡ ꯁꯦꯝꯒꯠꯅꯕꯥ ꯕꯦꯁ ꯀꯔꯀꯨꯃꯤꯟ
ꯀꯝꯕꯤꯅꯦꯁꯟ ꯊꯦꯔꯥꯄꯤꯁꯤꯡ
ꯀꯝꯕꯤꯅꯦꯁꯟ ꯗ꯭ꯔꯒ ꯄ꯭ꯔꯣꯗꯛꯇꯁꯤꯡꯒꯤꯗꯃꯛ ꯁ꯭ꯇꯦꯟꯗꯔꯗꯥꯏꯖꯗ ꯀꯔꯀꯨꯃꯤꯟ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯒ꯭ꯔꯦꯗ ꯁ꯭ꯄꯦꯁꯤꯐꯤꯀꯦꯁꯅꯁꯤꯡ
ꯑꯩꯈꯣꯌꯒꯤ ꯀꯔꯀꯨꯃꯤꯟ ꯑꯦꯛꯁꯠꯔꯦꯛꯠ ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯁ꯭ꯇꯦꯟꯗꯔꯗꯁꯤꯡ ꯄꯨꯔꯛꯄꯥ ꯑꯣꯏ
| ꯄꯦꯔꯥꯃꯤꯇꯔ | ꯁ꯭ꯇꯦꯟꯗꯔꯗ (95%) | ꯐꯥꯔꯃꯥ ꯒ꯭ꯔꯦꯗ (98%) | ꯃꯦꯊꯣꯗ |
|---|---|---|---|
| Curcuminoids Content | Min 95% | 95-98% | HPLC verified |
| Curcumin (as Curcumin I) | Min 70% | 75-80% | Primary active |
| Demethoxycurcumin | 15-25% | 15-20% | Secondary curcuminoid |
| Bisdemethoxycurcumin | 2-5% | 2-5% | Tertiary curcuminoid |
| Heavy Metals (Total) | <20 ppm | <10 ppm | ICP-MS tested |
| Lead (Pb) | <1.0 ppm | <0.5 ppm | Critical parameter |
| Arsenic (As) | <1.0 ppm | <0.5 ppm | ICP-MS |
| Cadmium (Cd) | <0.5 ppm | <0.3 ppm | ICP-MS |
| Mercury (Hg) | <0.5 ppm | <0.1 ppm | ICP-MS |
| Residual Solvents | Per ICH Q3C | Per ICH Q3C | GC-MS verified |
| Total Plate Count | <1,000 CFU/g | <100 CFU/g | Pharma limits |
| Yeast & Mold | <100 CFU/g | <10 CFU/g | Pharma limits |
| E. coli | Absent/g | Absent/10g | Enhanced testing |
| Salmonella | Absent/25g | Absent/25g | Mandatory |
| Aflatoxins (Total) | <10 ppb | <4 ppb | HPLC |
ꯁ꯭ꯄꯦꯁꯤꯐꯤꯀꯦꯁꯅꯁꯤꯡ ꯔꯦꯂꯦꯚꯦꯟꯠ ꯐꯥꯔꯃꯥꯀꯣꯄꯤꯌꯦꯜ ꯁ꯭ꯇꯦꯟꯗꯔꯗꯁꯤꯡꯒꯥ ꯀꯅꯐꯣꯔꯝ ꯇꯧꯏ
ꯀꯁ꯭ꯇꯝ ꯁ꯭ꯄꯦꯁꯤꯐꯤꯀꯦꯁꯅꯁꯤꯡ ꯔꯤꯀꯨꯑꯦꯁ꯭ꯠ ꯇꯧꯕꯤꯌꯨꯗꯣꯛꯌꯨꯃꯦꯟꯇꯦꯁꯟ ꯄꯦꯀꯦꯖ
ꯔꯦꯒꯨꯂꯦꯇꯔꯤ ꯁꯕꯃꯤꯁꯅꯁꯤꯡꯒꯤꯗꯃꯛ ꯄꯨꯝꯅꯃꯛꯀꯤ ꯗꯣꯛꯌꯨꯃꯦꯟꯇꯦꯁꯟ ꯁꯄꯣꯔꯠ
ꯔꯤꯀꯨꯑꯦꯁ꯭ꯠ ꯇꯧꯕꯗꯥ ꯑꯍꯦꯟꯕꯥ ꯗꯣꯛꯌꯨꯃꯦꯟꯇꯦꯁꯟ ꯐꯪꯕꯥ ꯌꯥꯏ
ꯗꯣꯛꯌꯨꯃꯦꯟꯇꯦꯁꯟ ꯄꯦꯀꯦꯖ ꯔꯤꯀꯨꯑꯦꯁ꯭ꯠ ꯇꯧꯕꯤꯌꯨꯀ꯭ꯕꯥꯂꯤꯇꯤ ꯁꯔꯇꯤꯐꯤꯀꯦꯁꯅꯁꯤꯡ
ꯑꯩꯈꯣꯌꯒꯤ ꯐꯦꯁꯤꯂꯤꯇꯤ ꯑꯃꯁꯨꯡ ꯄ꯭ꯔꯣꯁꯦꯁꯁꯤꯡ ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯏꯟꯗꯁꯠꯔꯤ ꯁ꯭ꯇꯦꯟꯗꯔꯗꯁꯤꯡ ꯄꯨꯔꯛꯄꯥ ꯑꯣꯏ
ISO 9001:2015
Quality management systems certification for consistent manufacturing processes
GMP Compliant
Good Manufacturing Practice compliance for pharmaceutical raw materials
FSSAI Licensed
Food Safety and Standards Authority of India registration
FDA Registered
US FDA facility registration for pharmaceutical ingredient supply
COA with Each Batch
Comprehensive Certificate of Analysis with full analytical data
DMF Support
Drug Master File documentation support available for regulatory submissions
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯁꯤꯖꯤꯟꯅꯕꯒꯤꯗꯃꯛ ꯄ꯭ꯔꯣꯗꯛꯇꯁꯤꯡ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯃꯦꯅꯨꯐꯦꯛꯆꯔꯔꯁꯤꯡꯒꯤꯗꯃꯛ ꯑꯩꯈꯣꯌꯒꯤ ꯄ꯭ꯔꯣꯗꯛꯠ ꯔꯦꯟꯖ
ꯀꯔꯀꯨꯃꯤꯟ ꯑꯦꯛꯁꯠꯔꯦꯛꯠ 95%
ꯈ꯭ꯋꯥꯏꯗꯒꯤ ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯑꯦꯄ꯭ꯂꯤꯀꯦꯁꯅꯁꯤꯡꯒꯤꯗꯃꯛ ꯁ꯭ꯇꯦꯟꯗꯔꯗꯥꯏꯖꯗ ꯀꯔꯀꯨꯃꯤꯅꯣꯏꯗ ꯑꯦꯛꯁꯠꯔꯦꯛꯠ
- 95% total curcuminoids
- Heavy metals <10 ppm
- Full COA with each batch
- MOQ: 100 kg
ꯀꯔꯀꯨꯃꯤꯟ ꯑꯦꯛꯁꯠꯔꯦꯛꯠ 98%
ꯈ꯭ꯋꯥꯏꯗꯒꯤ ꯍꯥꯏ ꯄꯨꯔꯤꯇꯤ ꯗꯔꯀꯥꯔ ꯑꯣꯏꯕꯥ ꯑꯦꯄ꯭ꯂꯤꯀꯦꯁꯅꯁꯤꯡꯒꯤꯗꯃꯛ ꯃꯦꯛꯁꯤꯃꯝ ꯄꯨꯔꯤꯇꯤ ꯑꯦꯛꯁꯠꯔꯦꯛꯠ
- 98% total curcuminoids
- Enhanced purity testing
- Stricter heavy metal limits
- MOQ: 50 kg
R&D ꯁꯦꯝꯄꯜ ꯄ꯭ꯔꯣꯒ꯭ꯔꯥꯝ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ R&D ꯇꯤꯝꯁꯤꯡꯒꯤꯗꯃꯛ ꯏꯚꯦꯜꯌꯨꯑꯦꯁꯟ ꯁꯦꯝꯄꯜꯁ ꯐꯪꯕꯥ ꯌꯥꯏ
R&D ꯁꯦꯝꯄꯜꯁ ꯔꯤꯀꯨꯑꯦꯁ꯭ꯠ ꯇꯧꯕꯤꯌꯨꯈꯪꯖꯤꯟꯈꯤ ꯍꯪꯕꯥ ꯋꯥꯍꯪꯁꯤꯡ
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯀꯝꯄꯦꯅꯤꯁꯤꯡꯅꯥ ꯑꯩꯈꯣꯌꯒꯤ ꯀꯔꯀꯨꯃꯤꯟꯒꯤ ꯃꯇꯥꯡꯗꯥ ꯈꯪꯖꯤꯟꯈꯤ ꯍꯪꯕꯥ ꯋꯥꯍꯪꯁꯤꯡ
What purity levels of curcumin do you offer for pharmaceutical use?
We offer curcumin extracts at 95% and 98% curcuminoid purity for pharmaceutical applications. The 95% grade is most common for general formulations, while 98% is used for applications requiring maximum purity. Both grades meet pharmacopeial standards.
Is your facility GMP certified?
Yes, our processing facility follows Good Manufacturing Practice guidelines. We maintain batch records, validated processes, and quality control procedures consistent with pharmaceutical raw material requirements. We can provide facility audit reports upon request.
Can you provide a Drug Master File (DMF)?
We provide DMF support documentation that can be incorporated into your regulatory filings. For US FDA submissions, we can prepare Type II DMF components. Timeline and specific requirements should be discussed with our regulatory team.
What is your minimum order quantity for pharmaceutical-grade material?
For pharmaceutical-grade curcumin extract, our minimum order is 100 kg. For standard turmeric powder used in pharmaceutical preparations, minimum is 1 MT. We can provide smaller quantities for R&D evaluation.
Do you provide stability data?
Yes, we conduct stability studies following ICH guidelines. Accelerated stability data (40°C/75% RH) and long-term stability data (25°C/60% RH) are available. We can also support stability studies for your specific formulations.
How do you ensure batch-to-batch consistency?
We maintain strict process controls, use consistent raw material sources from our own farms, and test every batch against established specifications. Our QC releases each batch only after full analytical verification. Batch records are maintained for complete traceability.
ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ ꯒ꯭ꯔꯦꯗ ꯀꯔꯀꯨꯃꯤꯟ ꯂꯧꯕꯤꯌꯨ
ꯄꯨꯝꯅꯃꯛꯀꯤ ꯗꯣꯛꯌꯨꯃꯦꯟꯇꯦꯁꯟꯒꯥ ꯂꯣꯌꯅꯅꯥ ꯐꯥꯔꯃꯥꯁꯨꯇꯤꯀꯦꯜ-ꯒ꯭ꯔꯦꯗ ꯀꯔꯀꯨꯃꯤꯟ ꯂꯧꯕꯤꯌꯨ
MOQ: 100 kg (ꯑꯦꯛꯁꯠꯔꯦꯛꯠ) | ꯂꯤꯗ ꯇꯥꯏꯝ: 2-4 ꯁꯅꯥ | ꯄꯦꯃꯦꯟꯠ: L/C, T/T