Pharmaceutical-Grade Curcumin
High-purity curcumin extracts and standardized turmeric for drug formulations, API manufacturing, and clinical research. GMP compliant with full documentation.
Curcumin in Pharmaceutical Applications
Curcumin's well-documented pharmacological properties make it a valuable compound for drug development and therapeutic applications.
Anti-inflammatory Activity
Extensively studied for COX-2 inhibition and NF-κB pathway modulation. Thousands of published studies support therapeutic potential.
Antioxidant Properties
Potent free radical scavenging and metal chelation properties. Supports formulations targeting oxidative stress conditions.
Research Interest
Active clinical research in oncology, neurology, cardiology, and metabolic disorders. Growing pipeline of curcumin-based therapeutics.
Quality Assurance Note
All pharmaceutical-grade materials undergo enhanced testing protocols including residual solvent analysis, extended heavy metals panel, and stricter microbiological limits. Each batch includes comprehensive documentation suitable for regulatory filings.
Pharmaceutical Applications
Our curcumin serves diverse pharmaceutical applications from formulation development to clinical research programs.
Drug Formulations
Curcumin as an active or adjunct ingredient in tablets, capsules, and oral preparations for anti-inflammatory and antioxidant applications
API Manufacturing
High-purity curcumin extract (95%+) as an Active Pharmaceutical Ingredient for proprietary drug development
Clinical Research
Standardized curcumin for clinical trials, pharmacokinetic studies, and therapeutic research programs
Topical Preparations
Curcumin for dermatological formulations, wound healing preparations, and topical anti-inflammatory products
Bioavailability Research
Base curcumin for developing enhanced bioavailability formulations using lipids, piperine, or nanoparticle technologies
Combination Therapies
Standardized curcumin for combination drug products and synergistic therapeutic formulations
Pharmaceutical-Grade Specifications
Our curcumin extract meets stringent pharmaceutical quality requirements. Custom specifications available for specific applications.
| Parameter | Standard (95%) | Pharma Grade (98%) | Method |
|---|---|---|---|
| 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 |
Specifications conform to relevant pharmacopeial standards. Custom testing protocols available for specific regulatory requirements.
Request Custom SpecificationsDocumentation Package
Complete documentation support for regulatory submissions and quality systems.
Additional documentation available upon request: facility audit reports, validation summaries, change control procedures.
Request Documentation PackageQuality Certifications
Our facility and processes meet pharmaceutical industry standards.
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
Products for Pharmaceutical Use
Our product range for pharmaceutical manufacturers and researchers.
Curcumin Extract 95%
Standardized curcuminoid extract for most pharmaceutical applications. Meets pharmacopeial specifications for drug formulations.
- 95% total curcuminoids
- Heavy metals <10 ppm
- Full COA with each batch
- MOQ: 100 kg
Curcumin Extract 98%
Maximum purity extract for applications requiring the highest curcuminoid concentration and strictest quality parameters.
- 98% total curcuminoids
- Enhanced purity testing
- Stricter heavy metal limits
- MOQ: 50 kg
R&D Sample Program
Evaluation samples available for pharmaceutical R&D. Contact us with your research requirements and application details.
Request R&D SamplesFrequently Asked Questions
Common questions from pharmaceutical companies about our curcumin products.
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.
Partner with a Reliable Curcumin Supplier
Get pharmaceutical-grade curcumin with complete documentation, consistent quality, and responsive technical support.
MOQ: 100 kg (extract) | Lead time: 2-4 weeks | Payment: L/C, T/T