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
Products
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
Post-marketing surveillance implementation
Support for PMS study setup and execution including site selection/contracting, monitoring, and database investigation.
Clinical research operations and monitoring
Study administration services including secretariat tasks, ethics committee coordination, contract management, and monitoring activities for clinical research and post-marketing trials.
Pre-market clinical trial consulting and liaison
Consulting and liaison services for pre-market clinical trials including support for multinational studies and overseas regulatory interactions.
Data management and biostatistics
Data management, statistical analysis and medical coding services for clinical trials, post-marketing surveys, and clinical research.
Medical writing
Preparation of study documents including survey protocols and final study reports.
Pharmacovigilance and safety management
Management of adverse-event information and safety reporting for clinical and post-marketing activities.
Post-marketing surveillance implementation
Support for PMS study setup and execution including site selection/contracting, monitoring, and database investigation.
Clinical research operations and monitoring
Study administration services including secretariat tasks, ethics committee coordination, contract management, and monitoring activities for clinical research and post-marketing trials.
Pre-market clinical trial consulting and liaison
Consulting and liaison services for pre-market clinical trials including support for multinational studies and overseas regulatory interactions.
Data management and biostatistics
Data management, statistical analysis and medical coding services for clinical trials, post-marketing surveys, and clinical research.
Medical writing
Preparation of study documents including survey protocols and final study reports.
Pharmacovigilance and safety management
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)