Documents

Trends in Coverage and Reimbursement Policies
Addressing the Outcomes Studies
FDA Review Patterns of DeNovo Submissions
Ethical Issues in Clinical Trials
Globalization of Clinical Trials

Study Management Services

Boston MedTech CRO specializes in the complete management of global clinical trials for medical devices and combination products. We know how to efficiently apply GCP and ICH requirements to yield FDA and CE acceptable data.
Study Management Services include:

Regulatory Interactions
Project Management
Data Safety Monitoring Board
Clinical Trial Monitoring
Data Management
Statistical Design and Analysis
Study Reports
Operations and Logistics