BME 695L Lecture 16: FDA and EPA Regulatory Issues

By James Leary

Biomedical Engineering, Purdue University, West Lafayette, IN

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Abstract

See references below for related reading.

16.1      Introduction and overview
16.1.1    How does the FDA think about nanomedical systems?
16.1.2    The 2006 Nanotechnology Task Force

16.2      Some details of the Nanotechnology Task Force Report
16.2.1    General findings of the report
16.2.2    Some initial recommendations of the Task Force
16.2.3    Where the FDA may need to meet EPA on nanoscale materials
16.2.4    Will FDA re-visit GRAS products containing nanomaterials?

16.3      How will the FDA consider nanomedical systems?
16.3.1    Nanomedical systems are integrated nanoscale drug and drug delivery devices
16.3.2    Either a drug or a device? How about a "Combination Product"?
16.3.3    Drug-Biologic combination products

16.4      Types of human clinical trials
16.4.1    IND
16.4.2    “Phase 0”
16.4.3    Phase 1
16.4.4    Phase 2
16.4.5    Phase 3
16.4.6    Phase 4

16.5      EPA and other regulatory agency issues
16.5.1    Assessing environmental impact of emerging nanotechnologies
16.5.2    Concept of life cycle assessment (LCA)
16.5.3    Toxicity of nanomaterials
16.5.4    Some recommendations of the 2006 International Conference on Nanotechnology and Life Cycle Assessment

16.6      Nanotechnologies and the workplace
16.6.1    NIOSH – Formulating workplace safety standards for nanotechnology
16.6.2    Protecting workers in the workplace
16.6.3    Assessing hazards in the workplace
16.6.4    Establishing a Nanotechnology Safety System

16.7      The future of nano-healthcare products

Credits

Copyright © 2011, James F. Leary, All rights reserved.

References

Commissioner of Food and Drugs "Nanotechnology Task Force Report 2007" FDA.gov July 25, 2007
"Environmental impact of nanotechnology documents: Life Cycle Assessments" NanotechProject.org
NIOSH Nanotechnology Research Center "Progress Toward Safe Nanotechnology in the Workplace" CDC.gov
Nano Healthcare Products Assessment. The Freedonia Group, Inc
Chinese FDA SFDA.gov.cn

Cite this work

Researchers should cite this work as follows:

  • James Leary (2011), "BME 695L Lecture 16: FDA and EPA Regulatory Issues," https://nanohub.org/resources/12498.

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Time

Location

1083 BME, Purdue University, West Lafayette, IN

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BME 695L Lecture 16: FDA and EPA Regulatory Issues
  • BME 695L Lecture 16: FDA, EPA, and NIOSH regulatory issues 1. BME 695L Lecture 16: FDA, EPA,… 8.5
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  • Relevance 2. Relevance 210.93333333333334
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  • For example: There is an 3. For example: There is an "FDA … 214.53333333333333
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  • 16.1 Introduction and overview 4. 16.1 Introduction and overview 258.26666666666665
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  • How does the FDA think about nanomedical systems? 5. How does the FDA think about n… 265.83333333333331
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  • A recent task force study making recommendation to the FDA regarding nanotechnology… 6. A recent task force study maki… 345.03333333333336
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  • The Task Force meeting… 7. The Task Force meeting… 420.43333333333334
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  • The official response to this task force report… 8. The official response to this … 638
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  • Task Force Mission… 9. Task Force Mission… 655.86666666666667
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  • 16.2 Some details of the Nanotechnology Task Force Report 10. 16.2 Some details of the Nanot… 708.26666666666665
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  • About the report… 11. About the report… 826.9666666666667
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  • General findings of the report… 12. General findings of the report… 991.8
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  • Some initial recommendations of the Task Force… 13. Some initial recommendations o… 1088.6666666666667
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  • Where FDA may need to meet EPA on nanoscale materials… 14. Where FDA may need to meet EPA… 1191.0333333333333
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  • Issue: Understanding Interactions of Nanoscale Materials with Biological Systems 15. Issue: Understanding Interacti… 1258.4333333333334
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  • Issue: Adequacy of Testing Approaches for Assessing Safety and Quality of Products Containing Nanoscale Materials 16. Issue: Adequacy of Testing App… 1340.7666666666667
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  • Perhaps the FDA will need to re-visit the safety of GRAS products containing nanomaterials? 17. Perhaps the FDA will need to r… 1568.2333333333334
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  • Products Not Subject to Premarket Authorization 18. Products Not Subject to Premar… 1662.2333333333334
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  • Recommendations for Consideration 19. Recommendations for Considerat… 1734.1666666666667
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  • 16.3 How will the FDA consider nanomedical systems? 20. 16.3 How will the FDA consider… 1854.9666666666667
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  • Nanomedical systems are integrated nanoscale drug and drug delivery devices that may present a new paradigm to the FDA 21. Nanomedical systems are integr… 2107.7
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  • Multilayered, Multifunctional Nanomedical Systems – A 22. Multilayered, Multifunctional … 2268.1
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  • CDER-FDA Jurisdiction of Nanomedical Systems? 23. CDER-FDA Jurisdiction of Nanom… 2396.4666666666667
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  • 16.4 FDA and Types of Clinical Trials 24. 16.4 FDA and Types of Clinical… 2443.8
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  • 16.4.1 Investigational New Drug (IND) Application 25. 16.4.1 Investigational New Dru… 2457
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  • Requirements for an IND Application 26. Requirements for an IND Applic… 2631.6666666666665
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  • 16. 4.2 Phase 0 (IND - microdosing) 27. 16. 4.2 Phase 0 (IND - microdo… 2743.2
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  • Phase I Clinical Trial in Humans 28. Phase I Clinical Trial in Huma… 2811.8333333333335
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  • 3 Types of Phase 1 Trials 29. 3 Types of Phase 1 Trials 2891.7333333333331
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  • Phase II Clinical Trials 30. Phase II Clinical Trials 3010.7666666666669
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  • Phase III Clinical Trials 31. Phase III Clinical Trials 3087.6
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  • Phase III Clinical Trials (continued) 32. Phase III Clinical Trials (con… 3246.5
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  • Phase IV trials (also known as Post Marketing Surveillance Trial) 33. Phase IV trials (also known as… 3329.7333333333331
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  • 16.5 EPA and other regulatory agency issues 34. 16.5 EPA and other regulatory … 3368.3
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  • Assessing the environmental impact of emerging nanotechnologies 35. Assessing the environmental im… 3589.2
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  • Little is currently known about the toxicity of nanomaterials 36. Little is currently known abou… 3647.4666666666667
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  • Some Recommendations of the International Conference on Nano-technology and Life Cycle Assessment, Washington DC, 2-3 October 2006 37. Some Recommendations of the In… 3713.6
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  • 16.6 Nanotechnologies and the workplace 38. 16.6 Nanotechnologies and the … 3773.2666666666669
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  • Nanotechnologies and the Workplace 39. Nanotechnologies and the Workp… 3938.0333333333333
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  • NIOSH (National Institute for Occupational Safety and Health) is attempting to formulate workplace safety standards 40. NIOSH (National Institute for … 3965.3666666666668
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  • Protecting Workers in the Workplace 41. Protecting Workers in the Work… 4080.9333333333334
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  • Assessing Hazards in the Workplace 42. Assessing Hazards in the Workp… 4197.1
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  • Establishing a Nanotechnology Safety System 43. Establishing a Nanotechnology … 4254.4666666666662
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  • 16.7 The future of nano-healthcare products 44. 16.7 The future of nano-health… 4268.8
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  • Nano Healthcare Products are Projected to Grow with Some Delays Due to Stringent Regulatory Barriers 45. Nano Healthcare Products are P… 4275.8666666666668
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  • References 46. References 4309.7666666666664
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