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, e.g.

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