Since July, 1st 2022, the Medical Research Involving Human Subjects Act (WMO) allows, under conditions,  subjects to be informed and asked for consent electronically. If electronic consent (eConsent) is to be used within a clinical study, it is mandatory to submit this completed checklist along with the research file to MREC NedMec. Submission of the Checklist is also required if the sponsor modifies an approved study to add the option for electronic consent (amendment).

Below here you can download the Dutch and English versions of the Checklist eConsent:

• A1. Checklist METC NedMec eConsent (NL)
• A1. Checklist METC NedMec eConsent (EN)

For further information on Electronic informed consent (eConsent) for METCs, see: https://www.ccmo.nl/metcs/documenten-voor-metcs/elektronische-toestemmingsverlening