Serious adverse event reporting in investigator-initiated clinical trials
Reporting adverse events (AEs) and serious AEs (SAEs) are practical steps to ensure safety for volunteers and patients in medical research involving medications, treatments and devices. However, the burden and cost of reporting should be proportionate with the public health benefit of this informati...
| Main Authors: | , , , |
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| Format: | Journal Article |
| Published: |
Australasian Medical Publishing
2016
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| Online Access: | http://hdl.handle.net/20.500.11937/20848 |