The laboratories that need good software most — clinical, translational, and research environments operating under real regulatory constraints — are also the least well served by the commercial software market. General-purpose tools require extensive customisation to be useful in domain-specific contexts. Highly specialised tools are typically built by small teams without the infrastructure to maintain them at institutional scale. Yashara exists in that gap. We develop and support software products that are domain-specific enough to be genuinely useful and institutionally robust enough to be relied upon.
| Product | Domain | Primary User | Core Function | Key Integrations |
|---|---|---|---|---|
| FluorocellAI | Imaging & Quantitative Biology | Cell biologists, microscopists, core facility staff | AI-driven fluorescence cell segmentation and high-throughput labeling | ImageJ, Fiji, OMERO, CellProfiler |
| ComplianceCall | Regulatory Compliance & Quality Management | Lab directors, technical consultants, QA officers | CLIA compliance lifecycle management — personnel, QC, instruments, surveys | FDA test database, CLIA Federal Register, CMS-116 |
| PuroChem | Chemical Safety & Hazard Intelligence | Chemical hygiene officers, safety coordinators, compliance staff | GHS hazard band tracking with temporal change history and toxicology profiles | SDS repositories, GHS databases, institutional EHS systems |
High-throughput AI cell labeling and segmentation for fluorescence microscopy.
Full Product PageFluorocellAI addresses one of the most labour-intensive bottlenecks in quantitative cell biology: the manual identification, labeling, and enumeration of cells within fluorescence microscopy images. By deploying purpose-trained deep learning segmentation models, FluorocellAI achieves single-cell resolution across densely populated fields, producing structured output data compatible with downstream statistical analysis pipelines.
The platform integrates as a native plugin within ImageJ and Fiji, preserving existing laboratory workflows while replacing the manual annotation step with AI inference. For core facilities and high-content screening applications, batch processing pipelines operate across multi-well plate formats with automated quality control flagging.
Comprehensive CLIA compliance management for clinical and research laboratories.
Full Product PageThe Clinical Laboratory Improvement Amendments regulatory framework imposes extensive documentation, personnel qualification, quality control, and proficiency testing requirements on laboratories of all sizes. ComplianceCall was designed with the direct participation of Technical Consultants, Laboratory Directors, and Quality Assurance officers to produce a platform that is both comprehensive in its regulatory coverage and practical in its daily operation.
The platform maintains a continuously updated connection to the CLIA Federal Register and the FDA test database, ensuring that changes to regulatory requirements surface automatically within the compliance dashboard rather than requiring manual review of regulatory publications.
GHS hazard band intelligence with longitudinal change tracking and toxicological depth.
Full Product PageThe Globally Harmonized System of Classification and Labelling of Chemicals establishes a structured framework for communicating chemical hazard information. PuroChem provides a curated, continuously maintained database of GHS hazard band classifications — with particular emphasis on the dimension most commonly absent from existing chemical management systems: the temporal history of classification changes.
When a chemical's hazard band is revised — whether due to new toxicological studies, regulatory review, or international harmonization updates — PuroChem records the change, preserves the prior classification, documents the basis for revision, and surfaces the delta to laboratory safety personnel with full toxicological context. This longitudinal perspective is essential for laboratories operating under OSHA Hazard Communication Standard obligations and institutional EHS compliance requirements.
Our scientific team provides structured demonstrations and trial access periods for qualified research teams and clinical laboratories.
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