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the name of the journal to wich the information from the study might be summitted for publication d3r3k420
the name of the journal to wich the information from the study might be summitted for publication d3r3k420
should informed consent be a process rather than a one time event
True, informed consent should be a process rather than a one-time event, since there are likely to be more than one aspect of a medical treatment about which a patient will need to be informed, and which will require consent.
Yes
If Dr. Bob can get informed consent without jeopardizing the life of the patient then he should do so. If stopping to get consent will risk the life of the patient then he should consider the consent implied and save the life.
the "informed consent" should consist of : 1.) procedure to be performed 2.) location of performance of planned procedure 3.) signature of physician 4.) signature of patient 5.) signature of "witness" (this could be parent/guardian if pt. is a minor, or perhaps the doctor's assistant.....someone in room who witnesses the signatures being written) Just so you know, and this is what confuses ALOT of patients....the informed consent DOES NOT have to itemize any possible complications or side effects of the planned procedure!!!
true
Many phone company websites have all sorts of information about buying a phone, the Samsung Intercept included. As well, your local phone stores should also have the information needed for making an informed purchase.
If the client themselves is incapable of giving their informed consent, a care-worker should secure the consent of an appropriate adult (preferably a member of the client's family).
No, a research participant has the right to withdraw from a study at any point even after giving informed consent. Researchers should respect the participant's decision to withdraw without any negative consequences.
Baptism should occur only when the party to be baptised is old and wise enough to make an informed decision on whether or not to consent.