The automation of clinical trial serious adverse event reporting workflow
نویسندگان
چکیده
منابع مشابه
Common data elements for secondary use of electronic health record data for clinical trial execution and serious adverse event reporting
BACKGROUND Data capture is one of the most expensive phases during the conduct of a clinical trial and the increasing use of electronic health records (EHR) offers significant savings to clinical research. To facilitate these secondary uses of routinely collected patient data, it is beneficial to know what data elements are captured in clinical trials. Therefore our aim here is to determine the...
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متن کاملIncreasing the Number of Adverse Drug Reactions Reporting: the Role of Clinical Pharmacy Residents
Detection of adverse drug reactions (ADRs) in hospitals provides an important measure of the burden of drug related morbidity on the healthcare system. Spontaneous reporting of ADRs is scare and several obstacles to such reporting have been identified formerly. This study aimed to determine the role of clinical pharmacy residents in ADR reporting within a hospital setting.Clinical pharmacy resi...
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ژورنال
عنوان ژورنال: Clinical Trials
سال: 2009
ISSN: 1740-7745,1740-7753
DOI: 10.1177/1740774509344778