When to include clinical study reports and regulatory documents in systematic reviews

When to include clinical study reports and regulatory documents in systematic reviews

Reporting bias is a major threat to the validity and credibility of systematic reviews. This article outlines the rationale for accessing clinical study reports and other regulatory documents (regulatory data) as a means of addressing reporting bias and identifies factors that may help decide whethe...

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Những tác giả chính:	Jefferson, T, Doshi, P, Boutron, I, Golder, S, Heneghan, C, Hodkinson, A, Jones, M, Lefebvre, C, Stewart, L
Định dạng:	Journal article
Ngôn ngữ:	English
Được phát hành:	BMJ Publishing Group 2018

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