Data sharing among data monitoring committees and responsibilities to patients and science.
Over the past three decades it has become increasingly recognized that systematic assessment of as high a proportion as possible of relevant research evidence is needed to protect the best interests of patients and the public. For example, this principle is manifested in clinical guidelines and, inc...
| Príomhchruthaitheoirí: | , , , , |
|---|---|
| Formáid: | Journal article |
| Teanga: | English |
| Foilsithe / Cruthaithe: |
2013
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Data sharing among data monitoring committees and responsibilities to patients and science.
Foilsithe / Cruthaithe 2013
Journal article