Medex15
Consultancy providing clinical and medical services for oncology and molecular diagnostics. Offers end-to-end support for clinical study development and execution (protocols, site selection, monitoring, data management, statistical analysis and reporting), medical affairs and publication support, and advisory board organization. Maintains a clinical trial portfolio and a publication record in oncology and diagnostic studies.
Industries
N/A
Nr. of Employees
small (1-50)
Services
End-to-end clinical study support including program/project management, clinical development plans, study design and execution (protocols, eCRF, site selection, regulatory submission, monitoring), and data analysis and clinical study report generation.
Medical affairs support, organization of advisory board meetings, scientific review of compounds and publication support including manuscript and abstract development.
Management and execution of clinical utility studies, prospective registries and observational studies, including enrollment management and end-of-study reporting.
End-to-end clinical study support including program/project management, clinical development plans, study design and execution (protocols, eCRF, site selection, regulatory submission, monitoring), and data analysis and clinical study report generation.
Medical affairs support, organization of advisory board meetings, scientific review of compounds and publication support including manuscript and abstract development.
Support for publication planning and execution; maintenance of a peer-reviewed publication record linked to clinical study activities.
End-to-end clinical study support including program/project management, clinical development plans, study design and execution (protocols, eCRF, site selection, regulatory submission, monitoring), and data analysis and clinical study report generation.
Medical affairs support, organization of advisory board meetings, scientific review of compounds and publication support including manuscript and abstract development.
Management and execution of clinical utility studies, prospective registries and observational studies, including enrollment management and end-of-study reporting.
End-to-end clinical study support including program/project management, clinical development plans, study design and execution (protocols, eCRF, site selection, regulatory submission, monitoring), and data analysis and clinical study report generation.
Medical affairs support, organization of advisory board meetings, scientific review of compounds and publication support including manuscript and abstract development.
Support for publication planning and execution; maintenance of a peer-reviewed publication record linked to clinical study activities.
Expertise Areas
- Clinical trial management
- Clinical development planning
- Oncology clinical research
- Molecular diagnostics and biomarker studies
Key Technologies
- Electronic Case Report Forms (eCRF) / electronic data capture
- Biostatistical analysis
- Gene expression profiling / molecular subtyping
- Microarray-based assays
News & Updates
Multiple peer-reviewed publications in oncology and molecular diagnostics, including work on gene expression profiling, molecular subtyping, and clinical utility studies.
Management and execution of clinical utility and registry studies (examples include PROMMIS, PROMIS, MINDACT and multiple prospective registries) with completed enrollments and published outputs.
Multiple peer-reviewed publications in oncology and molecular diagnostics, including work on gene expression profiling, molecular subtyping, and clinical utility studies.
Management and execution of clinical utility and registry studies (examples include PROMMIS, PROMIS, MINDACT and multiple prospective registries) with completed enrollments and published outputs.