Facilitating audits of clinical trial data using documents of the Food and Drug Administration
The Medical Review document of the FDA is a rich source of data about clinical trials underlying the approval of a given drug. There are also other sources of information about clinical trials, such as trial registries and publications. However the data in the various sources may be erroneous or dis...
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Hamilton Publishing, Inc.
2022-12-01
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| Reeks: | The Journal of Scientific Practice and Integrity |
| Online toegang: | https://doi.org/10.35122/001c.57582 |
| Tags: |
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