| Rebuttal to the letter to the editors regarding Heringa et al. (2020) | Regulatory toxicology and pharmacology | 18 hours | save |  |  |  |  |
| Heavy metal contamination in recorded and unrecorded spirits. Should we worry? | Regulatory toxicology and pharmacology | 18 hours | save | | | | |
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| Safety evaluation of Ochratoxin A and Citrinin after 28 days repeated dose oral exposure to Wistar rats | Regulatory toxicology and pharmacology | 17 days | save | | | | |
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| Response to “OECD 428 in vitro dermal absorption mass balance performance based on our in-house database of pesticide studies” | Regulatory toxicology and pharmacology | 28 days | save | | | | |
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| Safety evaluation of water extract of Gastrodia elata Blume: Genotoxicity and 28-day oral toxicity studies | Regulatory toxicology and pharmacology | 73 days | save | | | | |
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| A semi-automated workflow for adverse outcome pathway hypothesis generation: The use case of non-genotoxic induced hepatocellular carcinoma | Regulatory toxicology and pharmacology | 92 days | save | | | | |
| Rat two-generation reproductive toxicity and teratogenicity studies of a novel coccidiostat – Ethanamizuril | Regulatory toxicology and pharmacology | 111 days | save | | | | |
| “Natural” is not synonymous with “Safe”: Toxicity of natural products alone and in combination with pharmaceutical agents | Regulatory toxicology and pharmacology | 111 days | save | | | | |
| Chimeric hemagglutinin supra-seasonal universal influenza vaccine candidates administered sequentially by the intramuscular route are locally and systemically well-tolerated in rabbits | Regulatory toxicology and pharmacology | 111 days | save | | | | |
| Assessment of the inhibition risk of paris saponins, bioactive compounds from Paris polyphylla, on CYP and UGT enzymes via cocktail inhibition assays | Regulatory toxicology and pharmacology | 111 days | save | | | | |
| Comparison of the potential mechanisms for hepatotoxicity of p-dialkoxy chlorobenzenes in rat primary hepatocytes for read-across | Regulatory toxicology and pharmacology | 111 days | save | | | | |
| Opportunities for use of one species for longer-term toxicology testing during drug development: A cross-industry evaluation | Regulatory toxicology and pharmacology | 111 days | save | | | | |
| Evaluation of the sub-acute toxicity of Acacia catechu Willd seed extract in a Wistar albino rat model | Regulatory toxicology and pharmacology | 111 days | save | | | | |
| Phototoxic risk assessment of dermally-applied chemicals with structural variety based on photoreactivity and skin deposition | Regulatory toxicology and pharmacology | 118 days | save | | | | |
| A commentary on some epidemiology data for chlorpyrifos | Regulatory toxicology and pharmacology | 129 days | save | | | | |
| Development of improved QSAR models for predicting the outcome of the in vivo micronucleus genetic toxicity assay | Regulatory toxicology and pharmacology | 135 days | save | | | | |
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| Towards the development of an omics data analysis framework | Regulatory toxicology and pharmacology | 135 days | save | | | | |
| An evaluation framework for new approach methodologies (NAMs) for human health safety assessment | Regulatory toxicology and pharmacology | 142 days | save | | | | |
| Time extrapolation in regulatory risk assessment: The impact of study differences on the extrapolation factors | Regulatory toxicology and pharmacology | 148 days | save | | | | |
| Systematic review and meta-analysis of epidemiological literature evaluating the association between exposure to man-made vitreous fibers and respiratory tract cancers | Regulatory toxicology and pharmacology | 157 days | save | | | | |
| Determining the impact of flavored e-liquids on aldehyde production during Vaping | Regulatory toxicology and pharmacology | 157 days | save | | | | |
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| The accessibility of data on environmental risk assessment of pharmaceuticals – are environmental risk assessments information on emissions with respect to international and European environmental information law? | Regulatory toxicology and pharmacology | 177 days | save | | | | |
| Predicted Critical Environmental Concentrations for 500 Pharmaceuticals | Regulatory toxicology and pharmacology | 3598 days | save | | | | |
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