Working with data can be challenging. It is important to work with data sets that are understandable for you and for others. The following guidelines will help you to process your data in a proper way, so you will not get lost in your own data set, and others can find their way through your data set as well:
- Please note, that there are stricter requirements (trial master file and eCRF e.g.) for Clinical Trials with pharmaceuticals and Medical devices that fall under GCP regulation/ WMO-high/medium risk.