Individual data Summary (analysed) data
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Grey literature (press, newspaper, any kind of report, patent, technical report from government agencies or scientific research groups, working paper from research groups or committees, executive summary, book chapter, presentation at scientific conferences (abstracts, slides, posters), dissertation/ thesis, trial register entry, submission to regulatory authorities, database/statistical file*‡, regulatory drug trial reports) Full article published in a journal Regulatory documents (CSR (clinical study report), ISS (integrated summary of effectiveness or safety), PSURS (periodic safety updates), DAP (drug approval packages), EPAR (European public assessment report), CTD (common technical documents)) Study protocol, statistical analysis plan Case report forms Internal communication
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