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On August 8, 2007, the European Commission (EC) released the scientific opinion of the Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) on the appropriateness of the risk assessment methodology in accordance with the European Union’s (EU) technical guidance documents for new and existing substances for assessing the risks of nanomaterials. SCENIHR concluded that modifications to the existing technical guidance documents are necessary because special...

The EPA's recently released paper, TSCA Inventory Status of Nanoscale Substances -- General Approach, is important for developers of nanotechnologies. Nanomaterials that meet the Toxic Substances Control Act (TSCA) definition of "chemical substance" are subject to TSCA reporting requirements because they may exhibit properties different from the same substances in the bulk scale. A chemical substance means, in relevant part, "any organic or inorganic substance of a particular molecular...

The EPA's recently released paper, TSCA Inventory Status of Nanoscale Substances -- General Approach, is important for developers of nanotechnologies. Nanomaterials that meet the Toxic Substances Control Act (TSCA) definition of "chemical substance" are subject to TSCA reporting requirements because they may exhibit properties different from the same substances in the bulk scale. A chemical substance means, in relevant part, "any organic or inorganic substance of a particular molecular...

On August 1, 2007, the Nanoethics Group announced the release of a collection of papers entitled Nanoethics: The Ethical and Social Implications of Nanotechnology, which addresses issues related to nanotechnology’s impact on society. The anthology includes papers from nearly 40 experts worldwide and includes topics related to benefits, risk, environment, health, human enhancement, privacy, military, democracy, education, humanitarianism, molecular manufacturing, space...

On August 2, 2007, the U.S. Environmental Protection Agency (EPA) convened a public meeting on the Nanoscale Materials Stewardship Program (NMSP) under the Toxic Substances Control Act (TSCA). The meeting, which EPA had announced in a July 12, 2007, Federal Register notice, was well attended, with approximately 100 people in attendance. After introductory remarks by several EPA officials, various organizations presented their views on the NMSP and the associated...

On July 31, 2007, Representative Mike Honda (D-CA) introduced the Nanotechnology Advancement and New Opportunities (NANO) Act (HR 3235), which is intended to promote the development and responsible stewardship of nanotechnology in the U.S. Honda based the legislation on the recommendations of the Blue Ribbon Task Force on Nanotechnology, a panel of California nanotechnology experts with backgrounds in established industry, startup companies, consulting groups, non-profits,...

According to a recent survey presented at the Rural Futures conference in Canberra, Australia, nanotechnology in food and farming is inadequately regulated. Rural sociologist Dr. Kristin Lyons, Griffith University, stated: “Despite significant investment from the agrifood sector in nanotechnologies, the need for nano-specific regulation in this area hasn’t been recognised as a priority by the federal government.” Lyons said that the nano-agrifood industry will be...

On July 12, 2007, the U.S. Environmental Protection Agency (EPA) published in the Federal Register three separate notices related to the long-awaited Nanoscale Materials Stewardship Program (NMSP) under the Toxic Substances Control Act (TSCA). All of the notices and accompanying documents are available online.

On July 23, 2007, the United Kingdom (UK) Royal Society issued a press release entitled “’Responsible NanoCode’ for business to be developed.” The press release states: “An initiative to develop a ‘Responsible NanoCode‘ for businesses working with nanotechnologies has been launched by the Royal Society, Insight Investment, the Nanotechnology Industries Association and the Nanotechnology Knowledge Transfer Network today.” The Code is intended to establish a set of...

On July 19, 2007, the European Commission (EC) issued a press release entitled “Commission launches consultation on responsible research in Nanosciences and Nanotechnologies.” The press release states: “The European Commission has today announced a public consultation on responsible nanosciences and nanotechnologies research.  The consultation will provide input for a Recommendation to the Member States on a possible Code of Conduct for this emerging area of science, which...

On July 25, 2007, the Food and Drug Administration (FDA) Nanotechnology Task Force issued its report, which addresses regulatory and scientific issues and offers recommendations for each. The Task Force intends its report to outline ways for FDA to enhance its knowledge of nanotechnology to support its oversight for products using such technology, and to inform interested stakeholders what information may be needed to support the marketing of FDA-regulated products that use...

Environment Canada (EC) recently posted a New Substances Program Advisory Note entitled “Requirements for nanomaterials under the New Substances Notification Regulations (Chemicals and Polymers).” The Advisory Note was signed in June 2007 and states that the Canadian Environmental Protection Act, 1999 (CEPA) and the New Substances Notification Regulations (Chemicals and Polymers) (Regulations) “apply to new nanomaterials just as any other substance, whether a chemical or a...

On June 9, 2007, the U.S. Environmental Protection Agency (EPA) signed three Federal Register notices related to the Nanoscale Materials Stewardship Program (NMSP) under the Toxic Substances Control Act (TSCA) (appended). EPA intends to publish the notices in the July 12, 2007, Federal Register. The first notice announces a public meeting on August 2, 2007, to receive comments on the development of the voluntary NMSP. The second...

Until September 6, 2007, the European Commission (EC) Scientific Committee on Consumer Products (SCCP) is accepting comments on its Preliminary Opinion on the Safety of Nanomaterials in Cosmetic Products. According to the SCCP, traditional risk assessment methods — hazard identification, hazard characterization, and exposure assessment — may not be suitable for nanomaterials in cosmetics.  The SCCP suggests that either a new method should be developed, or...

In the July 2, 2007, Federal Register, the U.S. Environmental Protection Agency (EPA) published a notice regarding its conference entitled “Pollution Prevention through Nanotechnology,” which will be held on September 25-26, 2007, in Arlington, Virginia. EPA intends the conference to provide a forum to exchange ideas and information on using nanotechnology to develop new ways to prevent pollution. Lynn L. Bergeson is on the Steering Committee for the...

The American Bar Association’s (ABA) Section of Environment, Energy, and Resources (SEER) held its latest Nanotechnology Teleconference on June 21, 2007. Entitled “Nanotechnology and Environmental Governance,” the teleconference explored the need for voluntary environmental governance mechanisms to augment the U.S. Environmental Protection Agency’s traditional regulatory programs to manage the issues associated with nanotechnology. The teleconference featured three...

At its June 22, 2007, meeting, the National Toxicology Program’s (NTP) Board of Scientific Counselors (BSC) reviewed nominations of several substances for testing, including nanoscale silver. The Food and Drug Administration nominated nanoscale silver for toxicological studies “based on (a) increasing widespread use in drug, food and cosmetic products, and (b) the general lack of data on the toxicology and pharmacokinetics of these materials.” Comments on the...

The International Council on Nanotechnology (ICON) held a workshop entitled “Towards Predicting Nano-Bio Interactions” on June 5-7, 2007. The plenary presentations and meeting information are now online.

EHP-in-Press published an article entitled “Persistent Tissue Kinetics and Redistribution of Nanoparticles, Quantum Dot 705, in Mice: ICP-MS Quantitative Assessment.” The purpose of the study was to assess the tissue disposition and pharmacokinetics of quantum dots (QD705) in mice. According to the article, the plasma half-life of QD705 in mice was short (18.5 hours), but analyses revealed QD705 persisted and even continued to increase in the spleen, liver, and kidney 28...

On June 4, 2007, the Food and Drug Administration (FDA) announced a new advisory committee intended to counsel FDA on how to strengthen the communication of risks and benefits of FDA-regulated products to the public. The Risk Communication Advisory Committee will: Help FDA better understand the communication needs and priorities of the general public; Advise FDA on the development of strategic plans to communicate product risks and benefits; and Make recommendations to FDA on what...