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" Non-Therapeutic Biomedical Research Involving Human Subjects (Non-Clinical Biomedical Research) 1. In the purely scientific application of medical research carried out on a human being, it is the duty of the physician to remain the protector of the life... "
Code of Federal Regulations: Containing a Codification of Documents of ... - 90. lappuse
2001
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Code of Federal Regulations: Containing a Codification of Documents of ...

2000 - 440 lapas
...from criminal, civil and ethical responsibilities under the laws of their own countries. /. tluxic Principles 1. Biomedical research involving human...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1993 - 1052 lapas
...importance of the objective is in proportion to the Inherent risk to the subject. 5. Every biomedlcal research project involving human subjects should be...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999 - 372 lapas
...and should indicate that the principles enunciated in the present Declaration are complied with. II. Medical Research Combined with Professional Care (Clinical...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1995 - 1186 lapas
...medical research is justified by its potential diagnostic or therapeutic value for the patient. III. Non-Therapeutic Biomedical Research Involving Human...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1981 - 1252 lapas
...medical research carried out on a human being, it is the duty of the doctor to remain 80-059 O— 81 7 the protector of the life and health of that person...considerations related to the well-being of the subject. (v) An explanation as to how the research conformed to the principles of the declaration is provided,...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1996 - 1130 lapas
...duty of the physician to remain the protector of the life and health of that person on whom blomedical research is being carried out. 2. The subjects should...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 1120 lapas
...person on whom biomédical research is being carried out. 2. The subjects should be volunteers—ei-ther healthy persons or patients for whom the experimental...considerations related to the well-being of the subject. (Collection of Information requirements ap-proved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2001 - 398 lapas
...person on whom biomedical research is being carried out. 2. The subjects should be volunteers—either healthy persons or patients for whom the experimental...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1990 - 1086 lapas
...for whom the experimental design is not related to the patient's illness. 3. The investigator or the team should discontinue the research if in his/her...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1991 - 1218 lapas
...for whom the experimental design is not related to the patient's illness. 3. The investigator or the team should discontinue the research if in his/her...considerations related to the well-being of the subject. (Collection of information requirements approved by the Office of Management and Budget under control...
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