25 Apr 2013

  • Date:  April 25, 2013 
  • Time #1:  10:00am CEST   Register Now!
  • Time #2:  4:00pm CEST / 10:00am EDT / 9:00 am CDT    Register Now!
  • Duration:  1 hour
  • Language:  English
  • Cost:  Free
  • Presenter:  Dr. Marc Thouin

The regulations impacting new substance notification differ around the world and comprise a diverse set of obstacles including toxicological, environmental, and nanotechnological considerations. A clear understanding of the regulatory requirements is the key to enable you to bring your new ingredients to the global market.

First, the definition of the substance at hand needs to be well understood. Then the jurisdictions of the desired markets need to be defined, including volumes and uses. Once this is established, the data gaps are assessed in order to select viable options for filling such gaps. A good testing strategy can bring significant savings, for instance with read-across and waiver arguments to replace the need for de novo testing or by avoiding unnecessary study repeats, by choosing the correct study designs. A thorough notification dossier prompts acceptance by regulators and will ensure timely and successful product approvals.

Intertek helps clients bring new products to market in the timeliest and most cost-effective manner with regard to chemical regulatory compliance.

In a series of webinars, Intertek will bring Global Market Access understanding closer to you and how they impact your company. At the end there will be room for a Question & Answer session.

Topics to be addressed:

  • Overview of the chemicals regulations
  • Sharing practical experience
  • Intertek track record
  • Guidance on using testing facilities
  • Pitfalls to circumvent
  • Questions and answers

Who should attend?

  • Regulatory Affairs
  • Product Marketing, Development and Management
  • Product Compliance
  • Quality and Safety Management
  • Business Development
  • Supply chain management/ Purchasers


Please send your enquiry to events.regulatory@intertek.com