Conducting research with people requires proper considerations on every level. Therefore, it is important to follow these guidelines to make sure you will recruit the right population, randomize groups in the correct way, blind your participants as much as possible, etc:


  • 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.