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Pharmaceutical

Pharmaceutical development and manufacturing require rigorous quality control and precise characterization. Our analytical solutions support every phase from drug discovery to commercial production, ensuring compliance with regulatory standards while accelerating development timelines. We provide the tools you need for formulation development, quality assurance, and regulatory compliance.

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Key Capabilities

Drug formulation characterization
API purity and identity verification
Particle size and morphology analysis
Stability and degradation studies
Contamination detection
Regulatory compliance testing

🎯Our Solutions

Formulation Development

Particle analyzers and microscopy for optimizing drug delivery systems and bioavailability

Quality Control

Spectroscopy and chromatography systems for identity, purity, and potency testing

Contamination Analysis

Advanced imaging and elemental analysis for detecting and identifying foreign particles

Stability Testing

Long-term monitoring solutions for shelf-life determination and degradation studies

💡Challenges We Address

1

Challenge: Complex formulation characterization

Solution: Multi-modal analysis combining microscopy, spectroscopy, and particle size analysis

2

Challenge: Stringent regulatory requirements

Solution: Validated methods and 21 CFR Part 11 compliant software systems

3

Challenge: Identifying trace contaminants

Solution: Ultra-sensitive analytical techniques with ppm-level detection capabilities

🏆Success Stories

Accelerated FDA Approval

Comprehensive analytical data package enabled 6-month faster approval timeline

Manufacturing Quality Improvement

99.9% batch acceptance rate with enhanced quality control protocols

Ready to Get Started?

Let our experts help you find the perfect solution for your pharmaceutical applications.

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