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13:48 Aug 7, 2011 |
Arabic to English translations [PRO] Medical - Medical (general) / Consent Form | |||||||
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| Selected response from: sktrans Local time: 04:45 | ||||||
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Summary of answers provided | ||||
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5 | المشورة |
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5 | Ethan, either way is fine but I would say "consulted doctor" |
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4 | Informing physician advising physician |
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Discussion entries: 7 | |
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المشورة Explanation: الطبيب المستنصح : لقد قدنت النصاحح لهذا المريض حول طبيعة الاجراء The Arabic provided is inaccurate; the terms used are uncommon especially for a consent form which should be written in layman Arabic – MSA not classical Arabic, in addition to spelling error. قدمت الطبيب المستنصح – الطبيب المستشار Arabic is very similar to Hebrew - ייעוץ רפואי However in this context “advice” is inaccurate even in English, it should be “advise”, furthermore in Arabic this concept is always conveyed by using “explanation/instructions/information” , it is a “consent form” after all. However, if you insist on using “advise” then I would suggest the use of "المشورة" –" لقد قدمت المشورة لهذا المريض ..." |
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Ethan, either way is fine but I would say "consulted doctor" Explanation: مستنصح= some one who is asked for advise or I would say just "doctor" since we all go to the doc for advise anyway |
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Informing physician advising physician Explanation: Ethan- Do not do a word for word translation unless this is a backtranslation and you are checking on the translator. You have to use the proper terminology for the clinical research field . In order for a subject to participate in a trial/study, the physician who will conduct the study (the investigator) or his assistants (sub-investigators) have to inform and explain to all prospective study participants all the elements of the study (duration, number of participants, possible risks, who to contact in case of injury, etc.) so they can be "informed" and then agree or not to participate by signing or not signing the "Informed Consent Form". The investigator/sub-investigator has also to answer the subjects questions regarding the study and advise them about their queries. Azmi Jbeili has it right regarding: information/explanation etc. also that in order for a person to sign such a form, the person should understand it first. basically, it is the physician who comes to the patient with all the information ( since the doctor is recruiting subjects for his/her study) rather than the patient going to the physician for consultation. -------------------------------------------------- Note added at 6 hrs (2011-08-07 19:51:12 GMT) -------------------------------------------------- [PDF] VAMHCS Writing a VAMHCS Informed Consent Document HRP 03.02 www.maryland.research.va.gov/research/human/sops/0302.pdfFi... Format: PDF/Adobe Acrobat - Quick View The approved ICF must be viewed as a tool for informing potential subjects .... patient, the investigator needs to formally delegate this responsibility, ... -------------------------------------------------- Note added at 6 hrs (2011-08-07 19:52:40 GMT) -------------------------------------------------- [DOC] FILLING OUT THE INFORMED CONSENT FORM (ICF) irb.ufl.edu/docs/icf-instruct.docSimilar File Format: Microsoft Word - Quick View Investigators are reminded that the consent process is ongoing; subjects should continue to be informed throughout the research study and re-affirm consent ... Investigator and Investigator Site www.gcphelpdesk.com/index.../54-investigator-and-investigat... - CachedAccording to the ICH GCP what is the qualification for an Investigator? ... a person designated by the investigator, should fully inform the subject or, ... Is it requires mentioning the investigator name on the ICF as a contact person ... |
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