Chromatography Resins - High-Performance Separation Media
Industrial Premium
Pharmaceutical Ingredient

Chromatography Resins

Premium high-performance separation media engineered for demanding biotechnology applications including protein purification, monoclonal antibody production, vaccine manufacturing, and pharmaceutical processing. Our chromatography resins deliver exceptional selectivity, consistent performance, and reliable separation efficiency for critical biotechnology processes requiring superior purification media with stringent regulatory compliance standards.

  • High Separation Efficiency
  • Superior Selectivity
  • Pharmaceutical Grade
  • Consistent Performance
  • Protein Purification
  • Biotechnology Applications
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Technical Specifications

Product Type: Chromatography Resins (Mixed Bed)
Matrix: Cross-linked Agarose/Polyacrylamide
Particle Size: 45-165 μm (Wet)
Binding Capacity: ≥ 15 mg/mL (BSA)
pH Stability: 2-12 (Long term 3-10)
Flow Rate: 150-600 cm/h
Pressure Limit: 0.15 MPa (1.5 bar)
Temperature Stability: 4-30°C (Short term up to 40°C)
Storage Solution: 20% Ethanol
Endotoxin Level: ≤ 1 EU/mL
Microbial Count: ≤ 10 CFU/mL
Shelf Life: 3 years at 2-8°C
Packaging Options: 100mL, 500mL, 1L bottles

Applications

Protein Purification
Nucleic Acid Separation
Pharmaceutical Purification
Analytical HPLC
Preparative Chromatography
Research Applications

Industry-Specific Grades

DRAVYOM offers specialized chromatography resin grades tailored for different separation requirements, ensuring optimal performance and regulatory compliance.

Analytical Grade
Particle Size: 5-10 μm Resolution: High Flow Rate: 150-300 cm/h Application: HPLC analysis
Preparative Grade
Particle Size: 20-40 μm Capacity: High loading Scalability: Industrial Application: Large-scale purification
Pharmaceutical Grade
cGMP Manufactured: Yes Endotoxin: ≤ 1 EU/mL Documentation: Complete Application: Drug purification
Research Grade
Variety: Multiple chemistries Cost Effective: Optimized Flexibility: Diverse applications Application: Laboratory research

Quality Standards

DRAVYOM's Chromatography Resins are manufactured under cGMP conditions, meeting pharmaceutical and biotechnology standards for separation applications.

cGMP Certified Manufacturing
Pharmaceutical Grade Standards
≥ 15 mg/mL Binding Capacity
High Resolution Performance
Complete Performance Testing
Cold Chain Storage
Batch Documentation
Research Grade Support

Advanced Chemical Properties & Performance

Pharmaceutical Grade Chromatography Resins exhibit exceptional separation properties with superior selectivity and capacity characteristics for pharmaceutical purification applications. Their validated performance ensures reliable operation in drug manufacturing and regulatory compliance requirements.

Separation Properties
Binding Capacity: ≥50 mg protein/mL resin
Resolution: ≥1.5 between adjacent peaks
Selectivity: High target specificity
Recovery: ≥95% product recovery
Physical Properties
Particle Size: 50-150 μm
Pore Size: 300-1000 Å
pH Stability: 2-12 operating range
Chemical Stability: Sanitization compatible
Pharmaceutical Performance
Protein Purification: Monoclonal antibodies, enzymes
Drug Purification: API isolation and purification
Process Scalability: Lab to production scale
Validation Support: Complete documentation package
Composition Standards
Resin Purity: ≥99% active ligand
Endotoxin: ≤1 EU/mL
Heavy Metals: ≤5 ppm
Extractables: ≤10 ppm organic
Stability Properties
Shelf Life: 24 months (unopened)
Cycle Stability: ≥100 cleaning cycles
Storage Stability: 2-8°C storage
Sanitization: 0.1-0.5M NaOH compatible

Performance Characteristics

Performance metrics demonstrate Pharmaceutical Grade Chromatography Resins reliability in drug manufacturing with consistent quality, superior purification efficiency, and regulatory compliance for commercial pharmaceutical production.

Purification Efficiency

Purity: ≥99% target compound

Pharmaceutical grade purity
Drug Manufacturing

Yield: ≥95% product recovery

High process efficiency
Regulatory Compliance

Standards: USP/EP/JP compliance

Global regulatory acceptance
Process Economics

Cycles: ≥100 reuse cycles

Cost-effective operation
Quality Consistency

Variation: ±2% batch performance

Reliable production results
Process Time

Duration: Optimized cycle times

Efficient manufacturing

Safety Information

Pharmaceutical grade material requiring proper handling in controlled environments. Follow cGMP protocols with appropriate protective equipment, sterile handling procedures, and controlled access. Maintain documentation and traceability for regulatory compliance.

Pharmaceutical Grade
Sterile Handling
cGMP Required

Storage & Handling

Store in original pharmaceutical-grade containers in controlled temperature and humidity conditions. Maintain cold chain storage at 2-8°C and follow pharmaceutical storage protocols. Use validated storage equipment and maintain complete documentation for regulatory compliance.

Store at 2-8°C
Cold chain required
Complete documentation
Pharmaceutical protocols

Chemical Mechanisms & Reaction Pathways

Chromatography resins demonstrate controlled separation mechanisms through optimized molecular interactions, enabling predictable purification performance with well-characterized binding and elution properties for reliable pharmaceutical applications.

Binding Mechanisms

Specific molecular recognition with controlled binding kinetics

Primary separation mechanism
Selective Retention

Size exclusion and affinity-based separation principles

High selectivity purification
Ion Exchange

Controlled charge-based interactions for protein purification

pH-dependent separation control
Elution Control

Predictable desorption with optimized recovery conditions

Controlled product recovery

Regulatory Compliance & Documentation

Comprehensive regulatory compliance ensures pharmaceutical manufacturing standards with complete documentation packages supporting FDA, EMA, and global regulatory requirements for chromatography resin applications.

Pharmaceutical Standards

USP, EP, and JP compliance for pharmaceutical applications

cGMP Manufacturing

Current Good Manufacturing Practice compliance

Quality Systems

ICH guidelines and pharmaceutical quality management

Global Compliance

International pharmaceutical regulatory submissions

Documentation

Complete validation data and performance studies

Testing Protocols

Validated analytical methods and specifications

Technical Support & Value-Added Services

DRAVYOM's purification support team provides comprehensive guidance, method development, and technical expertise to optimize chromatography resin use in pharmaceutical purification and downstream processing applications.

Purification Support
  • Method development and optimization
  • Scale-up process consultation
  • Purification strategy design
  • Performance validation assistance
Manufacturing Services
  • Process development support
  • Equipment specification guidance
  • Quality control method transfer
  • cGMP compliance consultation
Regulatory Services
  • Validation protocol development
  • Regulatory submission support
  • Global compliance guidance
  • Audit preparation assistance
Supply Solutions
  • Custom packaging and labeling
  • Cold chain logistics management
  • Just-in-time delivery programs
  • Global distribution network

Environmental Impact & Sustainability

Our chromatography resin production emphasizes environmental responsibility through sustainable manufacturing practices, waste minimization, and comprehensive environmental impact management for pharmaceutical applications.

Resin Regeneration

Extended resin lifecycle with regeneration protocols

Water Management

Optimized buffer usage and water recycling systems

Clean Production

Energy-efficient manufacturing with emission controls

Waste Reduction

Minimized solvent usage and waste generation

Environmental Standards

ISO 14001 environmental management compliance

Sustainability Programs

Continuous improvement in environmental performance

Manufacturing Excellence & Quality Control

DRAVYOM's pharmaceutical manufacturing facility employs advanced production technology and quality monitoring systems to ensure consistent chromatography resin quality and performance across all production batches for pharmaceutical applications.

cGMP Production

State-of-the-art pharmaceutical manufacturing with controlled conditions

Highest quality standards for resin production
Performance Testing

Comprehensive testing including capacity, selectivity, and stability

Complete functional characterization
Quality Systems

ICH guidelines with pharmaceutical quality management

Regulatory compliant manufacturing processes
Cold Chain Packaging

Temperature-controlled packaging with complete documentation

Maintained integrity for pharmaceutical use

Market Applications & Performance Data

Comprehensive purification data demonstrating chromatography resin effectiveness across pharmaceutical applications with validated performance metrics and regulatory approval validation.

Pharmaceutical Purification
Recovery Rate: >95% product recovery Purity: >99% final product purity Reproducibility: ±2% batch variation
Protein Purification
Capacity: High binding capacity retention Selectivity: Superior separation performance Stability: 100+ cycle durability
Process Development
Scale-up: Predictable performance scaling Method Transfer: 98% success rate Technical Support: 96% customer satisfaction

DRAVYOM Competitive Advantages

Pharmaceutical Excellence

cGMP manufacturing with global regulatory compliance and pharmaceutical-grade quality standards

Purification Expertise

Advanced purification technology with method development and optimization support

Quality Assurance

Rigorous quality systems with complete validation documentation and performance guarantee

Cold Chain Excellence

Specialized logistics with temperature-controlled distribution and storage management

Technical Support

Expert purification guidance with method development and scale-up consultation services

Partnership Approach

Long-term pharmaceutical partnerships with comprehensive technical and regulatory support services