Investors from all over the world are interested in assessing whether nanomaterials and nanotechnology applications are being covered under applicable regulations, and if they are - how they are covered! This presentation by expert speaker Dr David Carlander focuses on how the US EPA and FDA, as well as the European Union are addressing nanomaterials and nanotechnology applications from a regulatory perspective. You will understand the specific regulatory aspects that are related to getting nanomaterials and products on to the markets. Dr David will also shed light upon the requirements of assembling a notification or authorization dossiers and the issues to consider due to a product's nano-specific properties.
In addition, you will learn about industries that are working in the nanotechnology field with nanomaterials or are creating products incorporating nanomaterials. Get knowledge and strategies to fulfill the requirements regulators (e.g. EPA/FDA and EU regulators) pose on nanomaterials. The presentation will focus on the chemical and raw materials sector but also cover other industries such as food, cosmetics and pharmaceuticals.
This webinar is a must-attend for people in the chemical manufacturing, paint, automotive, food and food packaging, cosmetics, pharmaceutical, paper, mineral, and photovoltaic manufacturing industries, as well as law firms.
Who Should Attend
Dr David Carlander
Dr David Carlander is the Director of Advocacy in the Nanotechnology Industries Association (NIA). In his position, he is covering the agricultural sector (food, feed, ag-chem) and REACH and risk assessment of nanomaterials. He is coordinating and participating in a number of various research projects and is representi... More info