Services

I offer advice in the following fields of drug development:

Clinical trial design

• Choice of design
• Sample size estimation
• Protocol writing
• CRF design

Data analysis

• Statistical analysis plans
• Design of tables, listings, and graphs
• Specifications of analysis datasets
• Programming and validation
• Data monitoring
• Preparation of (blind) data review

Presentation and interpretation of results

• Key results memos
• Clinical study reports
• Publications

Other statistical consultancy

• Support during drug submission
• Meta-analysis
• Support of IDMCs (independent data monitoring committees)
• Statistical training