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:''For use of this term in accounting, see .'' A source document is a document in which data collected for a clinical trial is first recorded. These data are usually later entered in the case report form. The ICH-GCP guidelines define source documents as "original documents, data, and records." Source documents contain source data, which is defined as "all information in original records and certified copies of original records of clinical findings, observations, or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial."〔 The FDA does not define the term "source document." == Examples of source documents == *Hospital records *Clinical and office charts *Laboratory notes *Memorandum *Subjects' diaries or evaluation checklists *Pharmacy dispensing records *Recorded data from automated instruments *Copies or transcriptions certified after verification as being accurate copies *Microfiches *Photographic negatives, microfilm or magnetic media *X-rays *Subject files *Records kept at the pharmacy, at the laboratories and at medico-technical departments involved in the clinical trial 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Source document」の詳細全文を読む スポンサード リンク
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