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T/CAAM 0002-2022 Active
T/CAAM 0002-2022 Record specification on adverse even in clinical trials of acupuncture and moxibustion
Abstract
This document stipulates the principles for recording adverse events in acupuncture clinical practice, the grading of the severity of adverse events, the recording and reporting of adverse events, and the methods for determining the correlation between adverse events and acupuncture therapies.
This document is applicable to the recording and reporting of information related to adverse events in acupuncture clinical research.
General Product Information
| Document Type | Group standards |
|---|---|
| Standard Status | Active |
| Standard Code | T/CAAM 0002-2022 |
| CCS | Medicine |
| ICS | Integrated medical science and healthcare devices |
| Implement Date | 2022-05-01 |
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$ 20.00
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$ 20.00