Getting started with CTIS data analysis in R
The guide is intended for anyone interested in working with publicly available CTIS data for analyses, statistics, and trend analysis of clinical trials. It demonstrates how to get and explore regulatory data in R, with examples focusing on approved clinical trials for a selected country.
The methodology was developed by Gothia Forum and has been used in the national report Overview of clinical drug trials in Sweden approved under EU Regulation No 536/2014, coordinated by Clinical Studies Sweden, which provides practical examples of how CTIS data can be analysed and presented.
Download the guide below and explore the report for further inspiration and examples.
Guide: Getting started with CTIS data analysis in R (PDF) pdf, 268 kB.