Synopses & Reviews
Synopsis
1. Introduction - History and Where We are Headed 2. Regulatory Guidance3. Sample Preparation and Biocompatibility Testing4. Testing for Leachables and Extractables5. Where the Data is - And What is It?6. Bridging Issues of Route7. Risk Assessments for Medical Devices8. (Q)SAR 9. Histopathology in Medical Device Studies10. Assessment of Nanomaterial Devices11. Integrated Safety Assessments for Devices12. Toxicity of Common Extractables and Leachables