IRB finds and documents that: (1) The research involves no more than minimal risk to the subjects; (2) The waiver or alteration will not adversely affect the rights and welfare of the subjects; (3) The research could not practicably be carried out without... Protecting Human Subjects: First Biennial Report on the Adequacy and ... - Side 96av United States. President's Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research - 1981 - 271 siderUten tilgangsbegrensning - Om denne boken
| 1993 - 1104 sider
...IRB finds and documents that: (1) The research involves no more than minimal risk to the subjects; (2) The waiver or alteration will not adversely affect...information after participation. (e) The informed consent require merits in this policy are not intended to preempt any applicable federal, state, or local laws... | |
| 2002 - 996 sider
...finds and documents that: (1) The research involves no more than minimal risk to the subjects; i2i The waiver or alteration will not adversely affect...additional Pertinent information after participation. («) The informed consent requirements in this policy are not intended to preempt any applicable federal,... | |
| 1996 - 1112 sider
...IRB finds and documents that: (1) The research involves no more than minimal risk to the subjects; (2) The waiver or alteration will not adversely affect...waiver or alteration; and (4) Whenever appropriate, the subject will be provided with additional pertinent information after participation. (e) The informed... | |
| 1998 - 500 sider
...IRB finds and documents that: (1) The research Involves no more than minimal risk to the subjects; (2) The waiver or alteration will not adversely affect...carried out without the waiver or alteration; and 14 CFR Ch. V (1-1-98 Edition) (4) Whenever appropriate, the subjects will be provided with additional... | |
| 1995 - 1144 sider
...IRB finds and documents that: (1) The research involves no more than minimal risk to the subjects; (2) The waiver or alteration will not adversely affect...welfare of the subjects; (3) The research could not bly be carried out without tt or alteration; and (4) Whenever appropriate, jects will be provided with... | |
| 1993 - 650 sider
...IRB finds and documents that: (1) The research involves no more than minimal risk to the subjects; (2) The waiver or alteration will not adversely affect the rights and welfare of the subjects; §11.116 Office of the Secretary of Transportation (3) The research could not practicably be carried... | |
| 2002 - 680 sider
...possible changes in methods or levels of payment for benefits or services under those programs; and (2) The research could not practicably be carried out without the waiver or alteration. (d) An IRB may approve a consent procedure which does not include, or which alters, some or all of... | |
| 1998 - 902 sider
...Possible changes in methods or levels of payment for benefits or serv-ices under those programs; and (2) The research could not practica-bly be carried out without the waiver or alteration. Vn ШВ may approve a consent .ure which does not include, or alters, some or all of the eleof informed... | |
| 2001 - 780 sider
...possible changes in methods or levels of payment for benefits or services under those programs; and (2) The research could not practicably be carried out without the waiver or alteration. (d) An ШВ may approve a consent procedure which does not include, or which alters, some or all of... | |
| Frank Harron - 1983 - 192 sider
...IRB finds and documents that; (1) The research involves no more than minimal risk to the subjects; (2) The waiver or alteration will not adversely affect the rights and welfare of the subjects; Informed Consent 133 (3) The research could not practicable be carried out without the waiver or alteration;... | |
| |