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. Author manuscript; available in PMC: 2020 Jul 31.
Published in final edited form as: Crit Rev Toxicol. 2018 Feb 23;48(5):359–374. doi: 10.1080/10408444.2018.1429386

Table 2.

Qualitative evaluation categories and criteria.

 Evaluation category Evaluation criteria
Characteristics Principle
Prediction (i.e. hazard vs. potency [categories or continuous])
Publication
Information sources
Input data Test method (in vitro and in chemico)
 - read-out used
 - validation status
 - reproducibility
 - issues (e.g. IP, availability)
In silico/expert system data/physicochemical properties
 - read-out used
 - availability
 - reliability
 - issues (e.g. IP, availability)
Expert knowledge
 - input used
 - availability
Principle
Prediction (i.e. hazard vs. potency [categories or continuous])
Publication
Information sources
Prediction algorithm Type
Availability
Transparency
Requirements for implementation (specific software)
Self-learning
Complexity
Sequential information generation
All inputs required?
Predictivity: Sample size (total and for categories)
Predictivity: Parameters (sensitivity, specificity, concordance)
Mechanistic relevance OECD AOP key events covered
Sequence of OECD AOP events considered
Justification/discussion of the mechanistic relevance
Applicability domain Chemical spectrum tested
Limitations (solubility, surfactants,...)
Potential limitations for cosmetic ingredients (e.g. natural extracts cannot be processed by in silico approaches)
Practical aspects Costs
Can be conducted by CRO?
Time required (per substance)