Use the "Model Proefpersoneninformatie" in order to obtain your explicit and informed consent
When your study is subject to the WMO you are obliged to use the “Model Proefpersoneninformatie”. In this template, which has been developed by the Central Committee on Research Involving Human Subjects (CCMO), an informational part and an explicit consent part are integrated which is also known as an Informed consent template.
Also for non-WMO research (for example observational studies) it is strongly advised to use the Model Proefpersoneninformatie in order to obtain your explicit and informed consent.
For more detailed information please visit the CCMO website or the website of the METC of the MUMC+.