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Getting Nanomaterials to the Market - What Regulations Should I Worry About? (CHM250A)

Presented by: Dr David Carlander
(*) Single User Price. For multiple users please call 1-844-384-4744
Pre Recorded Webinar
60 minutes
Event Description
See the sneak peek before you buy!
1.0 CM

Learn About US EPA, FDA and EU Regulations on Nanomaterials and Nanotechnology Applications

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.

Training Highlights:

  • Steps and considerations nanotechnology industries need to take to get their products onto the market following applicable legislations
  • Current nanospecific requirements regulators (e.g. FDA/EPA/EU) pose for nanomaterials
  • Current status of common international risk assessment procedures, covering e.g. the latest OECD discussions
  • The latest US/EU and international regulatory developments and their impacts on industry based on the NIA's worldwide regulatory monitoring database
  • Strategies to develop valid nano-specific information of regulatory relevance

Who Should Attend

  • Experts working with nanomaterials
  • Innovation Managers
  • Product Developers
  • Products Stewardship Managers
  • Sales Managers
  • Executive Directors
  • Lawyers
  • Risk Assessors
  • Regulatory Affairs Manager
  • Scientific Officers
  • Research Scientists
  • Materials Manager
  • Compliance Officer
  • EHS Director
About Our Speaker(s)

Dr David Carlander | Nanomaterials Risk Assessment  SpeakerDr 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

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    Event Title: Getting Nanomaterials to the Market - What Regulations Should I Worry About?
    Presenter(s): Dr David Carlander

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