17:44 Oct 20, 2019 |
German to English translations [PRO] Medical - Medical (general) | |||||||
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| Selected response from: David Hollywood Local time: 08:02 | ||||||
Grading comment
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Summary of answers provided | ||||
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3 +2 | researchers presenting their findings |
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3 | authors |
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1 | competent regulatory agencies / authorities for clinical study findings |
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competent regulatory agencies / authorities for clinical study findings Explanation: The scientific use of the clinical study findings requires their approval by the competent regulatory agencies / authorities. sources: Regulatory Issues for Clinical Trials in Humans https://academic.oup.com › epirev › article-pdf JF Collins - 2002 - Clinical trials in humans are research studies designed to evaluate two or more ... the research actually takes place, and federal and state regulatory agencies have .... Statement that subjects will be provided any new findings that may relate to ... Guidelines on Regulating the Conduct of Clinical Trial in ... apps.who.int › medicinedocs › documents Bodies having the power to regulate. In the ICH GCP guideline the expression Regulatory Authorities includes the authorities that review submitted clinical data Page 11 and those that conduct inspections (see 1.29). These bodies are sometimes referred to as competent authorities. Good Clinical Practice (GCP) Inspections - HPRA www.hpra.ie › medicines › regulatory-information › clinical-trials › good-... The regulations require that all clinical trials covered by the provisions of the ... be received from the Competent Authority of another EU member state or the .... These may become graded findings depending on the nature of the clarification. -------------------------------------------------- Note added at 5 hrs (2019-10-20 23:00:57 GMT) -------------------------------------------------- Glad to have been of help! |
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researchers presenting their findings Explanation: I would suggest |
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14 hrs confidence:
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