Experience Geneuity Clinical Trial Study Support
Geneuity offers advanced clinical research services focused on improving patient health. Board certified professionals in molecular diagnostics, cytogenetics and hematopathology are available in house to assist in the development and review of study protocols. Our clinical trial research experts are experienced with document requirements, data and report management, specimen handling and storage concerns associated with complex clinical trials studies. Geneuity delivers standardized results bringing together expertise in oncology, hematopathology, clinical research and clinical services providing you with solid clinical trial evidence.
Therapeutic Experience and Clinical Trial Testing
Partnering with a leader in genomic medicine with more than 25 years of experience in molecular diagnostics and more than 10 years in research services brings expert knowledge and application in molecular diagnostic assay development, clinical testing and bioinformatics. Geneuity delivers timely results for an expedient regulatory submission ensuring minimal trial cost and better outcomes.
Experience Geneuity Diagnostic and Medical Device Validation
Experience in Molecular Diagnostics as a Clinical Reference laboratory for more than 25 years brings expertise to conducting medical diagnostic validation testing. Access to sample types, bioinformatics and pathology consultation ensures timely results and shorter time to regulatory submission. We serve Oncologists, Pathologists and Women’s Health Physicians with a broad menu of specialty pathology and molecular testing. We are experienced in data collection for IVD/PMA submission as well as data presentations for FDA advisory committees.
Conducting assays in
- Molecular and Anatomic Pathology
- Quantitative PCR
- Gene sequencing
- 5 to 10 color flow cytometry
- Constitutional and Oncology cytogenetics with karyotype analysis
- Fluorescence in-situ hybridization
- Immunohistochemistry and special stains
- Chromogenic In-situ hybridization



