Serious adverse event reporting in investigator-initiated clinical trials

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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...

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Bibliographic Details
Main Authors:	Wallace, S., Myles, P., Zeps, Nikolajs, Zalcberg, J.
Format:	Journal Article
Published:	Australasian Medical Publishing 2016
Online Access:	http://hdl.handle.net/20.500.11937/20848

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