Planning |
Composition of a skilled review team covering all fields of expertise required, especially systematic review experience |
Definition of the role of the systematic review sponsor |
Framing the question |
Framing of the question in a way that it is amenable to systematic reviews |
Developing and publishing of the protocol |
Publication of protocols so that they are highly and timely visible to stakeholders and interested parties |
Searching for evidence |
Identification of sources to be searched, including gray literature sources |
Provision of means to conduct appropriately balanced searches, e.g., by better annotation of the toxicological literature |
Familiarization of information specialists with toxicological evidence and databases |
Selecting the evidence |
Handling of the possibly vast amount of identified records and appropriate documentation of the selection process |
Extracting (the data) |
Efficient and transparent data management |
Assessing the evidence |
Determination of the importance of the various potential quality aspects, e.g., by empirical evidence |
Determination on how to best to integrate quality appraisal results into developing and supporting conclusions |
Analyzing data |
Exploration of the role of publication bias in toxicology, i.e., the frequency, the direction and the causes |
Exploration of the use of investigating external validity of subgroups |
Interpreting the results |
Determination of the confidence in a body of evidence |
Exploration of how to integrate bodies of evidence within an evidence stream and across evidence streams |
Reporting |
Making available all information relevant to allow for independent replication of the review |