Description
CLARITTY PARTICLE
– Key Capabilities;
1) Particle Size, Shape & Morphology Profiling
- Quantify parameters length, width, circularity, solidity, spherecity, surface are, texture, feret diameters, and are for precise material evaluation.
2) Semi-Automated Particulate Matter Assessment
- Supports particle counting in injectable and suspension-based samples following
global pharmacopeial guidelines. Manual validation is enhanced through 21 CFR Part 11 Application, overlays, and interactive image processing.
3) Multi-Class Component Differentiation
- Distinguish APIs, excipients, agglomerates, and foreign matter using intelligent AI-based classification.
4) Low-Contrast & Transparent Particle Enhancement
- Improve visibility and boundary detection for faint or translucent particles—essential in emulsions, gels, and nano formulations.
– Key Features;
1) CFR Part 11-Ready Architecture
- Full compliance with regulatory frameworks through e-signatures, audit trails, controlled access, and data integrity protocols.
2) High-Throughput Workflow Support
- Batch processing tools reduce turnaround time for QC and method development teams.
3) Semi-Automated Imaging Workflow
- Easily integrates with optical and digital microscopes for consistent image acquisition and repeatable results.
4) Detailed Reporting & LIMS Integration
- Generate customizable, audit-ready reports with measurement overlays, metadata, and export formats compatible with most laboratory systems.
Applications Include;
- API particle analysis in R&D and
- Excipient and blend characterization
- Globule size distribution in creams, emulsions, and ointments
- Foreign matter examination in complaint investigations
- Particle size and shape analysis in deformulation studies.



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