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Why "study subject" Instead of "study participant"?
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For human clinical trials, there is a growing movement to replace the term "study subject" with a terminology that is more respectful and recognizes the agency of those who consent to be treated and have their data collected. The term "participant”, rather than "study subject", is now used in ICH E6 R3 guidelines. The TransCelerate Biopharma Common Protocol Template states that "participant" may be used in patient-facing documents.

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Japan CCCIDM SMIS: Medical History, Family History, and Age of Symptom Onset
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Japan Clinical Informatization for Chronic Diseases Related to Lifestyle

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Japan CCCIDM SMIS: Vital Signs
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Japan Clinical Informatization for Chronic Diseases Related to Lifestyle

Standard(s)SDTMIG, Controlled Terminology
Japan CCCIDM SMIS: Smoking
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Japan Clinical Informatization for Chronic Diseases Related to Lifestyle

Standard(s)SDTMIG, Controlled Terminology
Japan CCCIDM SMIS: Laboratory Data
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Japan Clinical Informatization for Chronic Diseases Related to Lifestyle

Standard(s)SDTMIG, Controlled Terminology
Japan CCCIDM SMIS: Dental Clinic Visit
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Japan Clinical Informatization for Chronic Diseases Related to Lifestyle

Standard(s)SDTMIG, Controlled Terminology
Japan CCCIDM SMIS: Electrocardiogram (ECG)
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Japan Clinical Informatization for Chronic Diseases Related to Lifestyle

Standard(s)SDTMIG, Controlled Terminology