Technical documentation for clinical evaluation.
Resources for clinicians, embryologists, and laboratory directors performing scientific or operational due diligence on MicroSort.
Gated Technical Downloads
Select a resource to request access. All files are distributed in PDF format.
Methodology white paper
Validation protocol summary
Workflow integration guide
Sample-quality requirements specification
Cryopreservation and shipping protocol
Quality-assurance framework
Clinical Evaluation Framework
A structured guide for clinicians performing scientific due diligence on MicroSort technology.
1. Key Evaluation Criteria
Assess sorting efficiency (validated at 94.4% for X-chromosome enrichment), post-sort total motile sperm count recovery, and cell viability under low operating sheath pressures (< 1 PSI).
2. What to look for in documentation
Review DNA integrity index datasets (COMET assay values), fluid system layout blueprints, and multi-center clinical trials published in peer-reviewed journals.
3. Clinical introduction call structure
The 30-minute introductory session covers hardware footprints, embryologist training timelines, validation run checklist parameters, and custom regional licensing agreements.
Schedule a Clinical Introduction
Discuss installation specifications, validation checklists, and research datasets directly with our clinical affairs team.