What actions are required to be done by the site staff and the monitor -according to GCP- if the signed informed consent was lost?
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What actions are required to be done by the site staff and the monitor -according to GCP- if the signed informed consent was lost?
There is a reply to this by the MHRA Moderator and by me (both in agreement) on missing consent forms, in the section/thread called "Investigator Site" or similar.