Meditrix
Meditrix Corporation is dedicated to creating the future with Real World Evidence. They contribute to maximizing the value of Real World Data through clinical studies and post-marketing surveys. The company has extensive experience in medical devices and offers efficient business development services. They operate in clinical research organization (CRO), digital health, and strategic consulting sectors, providing systems for post-marketing surveys and clinical trials, data science, and quality management. Their mission is to support healthcare through innovative systems and data management, with a focus on reliability, security, and future integration.
Industries
Nr. of Employees
small (1-50)
Meditrix
Patents
System and method for providing virtual reality contents for relaxation training to stabilize psychological state of user
US-12613569-B2
View Details
System and method for providing virtual reality contents for relaxation training to stabilize psychological state of user
US-12613569-B2
View DetailsProducts
Integrated clinical research systems (registration/randomization, CTMS, EDC, CDMS)
Suite of systems supporting registration/randomization, clinical trial management, electronic data capture, and clinical data management for post-marketing surveys and clinical trials.
Integrated clinical research systems (registration/randomization, CTMS, EDC, CDMS)
Suite of systems supporting registration/randomization, clinical trial management, electronic data capture, and clinical data management for post-marketing surveys and clinical trials.
Services
Support for PMS study setup and execution including site selection/contracting, monitoring, and database investigation.
Study administration services including secretariat tasks, ethics committee coordination, contract management, and monitoring activities for clinical research and post-marketing trials.
Consulting and liaison services for pre-market clinical trials including support for multinational studies and overseas regulatory interactions.
Data management, statistical analysis and medical coding services for clinical trials, post-marketing surveys, and clinical research.
Preparation of study documents including survey protocols and final study reports.
Management of adverse-event information and safety reporting for clinical and post-marketing activities.
Support for PMS study setup and execution including site selection/contracting, monitoring, and database investigation.
Study administration services including secretariat tasks, ethics committee coordination, contract management, and monitoring activities for clinical research and post-marketing trials.
Consulting and liaison services for pre-market clinical trials including support for multinational studies and overseas regulatory interactions.
Data management, statistical analysis and medical coding services for clinical trials, post-marketing surveys, and clinical research.
Preparation of study documents including survey protocols and final study reports.
Management of adverse-event information and safety reporting for clinical and post-marketing activities.
Expertise Areas
- Post-marketing surveillance (PMS) management
- Clinical trial management and monitoring
- Real-World Evidence and registry studies
- Medical device clinical development
Key Technologies
- Electronic Data Capture (EDC)
- Clinical Trial Management System (CTMS)
- Randomization/assignment systems
- Clinical Data Management System (CDMS)
News & Updates
We have started full-function research management for a large-scale registry involving 68 facilities and 1,500 to 2,000 cases, emphasizing the importance of Real World Data utilization.
We have started full-function research management for a large-scale registry involving 68 facilities and 1,500 to 2,000 cases, emphasizing the importance of Real World Data utilization.