assess scientific literature and data on general nanomaterials interactions with biological systems and on specific nanomaterials of concern to the Food and Drug Administration;

in cooperation with other Federal agencies, develop and organize information using databases and models that will facilitate the identification of generalized principles and characteristics regarding the behavior of classes of nanomaterials with biological systems;

promote Food and Drug Administration programs and participate in collaborative efforts, to further the understanding of the science of novel properties of nanomaterials that might contribute to toxicity;

promote and participate in collaborative efforts to further the understanding of measurement and detection methods for nanomaterials;

collect, synthesize, interpret, and disseminate scientific information and data related to the interactions of nanomaterials with biological systems;

build scientific expertise on nanomaterials within the Food and Drug Administration, including field and laboratory expertise, for monitoring the production and presence of nanomaterials in domestic and imported products regulated under this Act;

ensure ongoing training, as well as dissemination of new information within the centers of the Food and Drug Administration, and more broadly across the Food and Drug Administration, to ensure timely, informed consideration of the most current science pertaining to nanomaterials;

encourage the Food and Drug Administration to participate in international and national consensus standards activities pertaining to nanomaterials; and

carry out other activities that the Secretary determines are necessary and consistent with the purposes described in paragraphs (1) through (8).