I rise today with Senator Cardin to introduce the Nanotechnology Safety Act of 2010 which will authorize a program of scientific investigation by the Food and Drug Administration on nanotechnology-based medical and health products. Nanotechnology holds great promise to revolutionize the development of new medicines, drug delivery, and orthopedic implants while holding down the cost of health care. However, Congress and the FDA must assure the public that nanotechnology-based products are both safe and efficacious. The Nanotechnology Safety Act of 2010 will enable the FDA to properly study how nanomaterials are absorbed by the human body, how nanomaterials designed to carry cancer fighting drugs target and kill tumors, and how nanoscale texturing of bone implants can make a stronger joint and reduce the threat of infection. Nanotechnology, or the manipulation of material at dimensions between 1 and 100 nanometers, is a challenging scientific area.
Mark Pryor: “I rise today with Senator Cardin to introduce the Nanotechnology Safety Act of 2010 which will authorize a program of…”
Editor's note · Context
The speaker is introducing the Nanotechnology Safety Act of 2010 to ensure the safety of nanotechnology-based health products.
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