Regulatory documents used as a basis for the eClinical Forum eSource Readiness Assessment (eSRA)
eCF eSRA Release 2023 is based on regulatory documents from FDA (USA), EMA (European Union), PMDA (Japan), CMPS (China), MHRA (UK) and ICH (International). The eClinical Forum will continue to monitor new releases and updates of regulatory documents from these agencies to determine if the eSRA template questions should be updated.