Documents
Study Management Services
Study Reports
Properly reporting clinical trial data is required to achieve multiple goals, from regulatory submissions to marketing activities, supporting reimbursement development campaigns and claims about the benefits of using the device in clinical practice. Boston MedTech CRO’s extensive knowledge of the medical device industry uniquely positions us to provide comprehensive report preparation services. All reports are customized, based on client needs, such as:
- Interim and final study reports
- Regulatory submissions
- Marketing activities
- Reimbursement campaigns
- Scientific publications
Reports cover all aspects of the clinical trial including study design, patient assessment, demographics, data analysis, study outcomes, medical device performance, risk/benefit analysis, device safety and effectiveness, adverse events occurrences and other relevant issues.