During the US, the FDA can audit the information of local website investigators after they have completed participating in a study, to determine whenever they had been properly following study treatments. This audit could be random, or for cause (since the investigator is suspected of fraudulent details). Avoiding an audit https://patient-recruitment-for-c92457.amoblog.com/the-smart-trick-of-clinical-trial-volunteers-needed-that-no-one-is-discussing-48398633