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1. Critical aspects in dissolution testing of nanomaterials in the oro-gastrointestinal tract: the relevance of juice composition for hazard identification and grouping

2. Regulatory safety assessment of nanoparticles for the food chain in Europe

3. “Advanced materials” and the challenges on the horizon for testing their (eco)toxicity and assessing their hazard

4. Grouping of orally ingested silica nanomaterials via use of an integrated approach to testing and assessment to streamline risk assessment

6. Integrated approaches to testing and assessment for grouping nanomaterials following dermal exposure

11. An integrated approach to testing and assessment of high aspect ratio nanomaterials and its application for grouping based on a common mesothelioma hazard

13. Possible Adverse Effects of Food Additive E171 (Titanium Dioxide) Related to Particle Specific Human Toxicity, Including the Immune System

14. A framework for grouping and read-across of nanomaterials- supporting innovation and risk assessment

17. Nanomaterial grouping: Existing approaches and future recommendations

20. Towards a nanospecific approach for risk assessment

24. Horizon scan of nanomedicinal products

30. Concern-driven integrated approaches to nanomaterial testing and assessment – report of the NanoSafety Cluster Working Group 10

31. Considerations on the EU definition of a nanomaterial: Science to support policy making

34. Presence of Nano-Sized Silica during In Vitro Digestion of Foods Containing Silica as a Food Additive

36. Presence and risks of nanosilica in food products

37. Nano-silver – a review of available data and knowledge gaps in human and environmental risk assessment

39. Comparison of five in vitro digestion models to in vivo experimental results: Lead bioaccessibility in the human gastrointestinal tract

43. Comparison of Five In Vitro Digestion Models To Study the Bioaccessibility of Soil Contaminants

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