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Cosmetics Safety Seminar

Dates:
7 March 2012 - Leicester
19 September 2012 - Leicester

Course Leader:
Dr Mabel Iwobi

Duration:
Full Day

Overview
A primary requirement in the manufacture of safe cosmetic products is protecting the health of the consumer from harm. This protection also enables increased consumer confidence.

Knowledge, understanding and interpretation of the law governing the manufacture and marketing of cosmetic products are principally the role and responsibilities of the manufacturer, importer and distributor. However, help is available. Since the first law governing the manufacture and marketing of safe cosmetic products was introduced in the European Union (EU) in 1976 in the form of a Directive (76/768/EEC), and each Member State transposed (interpreted) it into their own Regulation, a number of changes in the form of amendments had also occurred. Keeping up-to-date with these changes is very important. A Safety Assessor can help to guide and provide interpretation of the cosmetics legislation.

Starting on the 11th July 2013, the EU Directive will be replaced by the Regulation (EC) 1223/2009 which will apply directly across all the EU Member States. Additional improved changes have also been enacted. This new Cosmetics Regulation (also known as the Recast) becomes law on 11th July 2013. How prepared are you?

The morning session will examine the Cosmetics Directive with specific emphasis on what information is needed before a cosmetic product can be legally sold in the EU, what is regulated, comparison with the new Regulation, identifying the new changes and addressing the cosmetic products labelling requirements. Simple practical exercises will be used to illustrate relevant points.

In the afternoon session, an insight will be given into the processes involved in the cosmetic safety assessment. There will be a review of the type and quality of data/information required and available; also the additional requirements of the new Regulation. The relationship between hazard, exposure and risk, and how these are expressed with regards to types of products will be considered. At Intertek, we aim to help prevent potential adverse consequences and provide a solution..

Agenda 

  • Arrival & Refreshments
  • Introduction to the EU Cosmetic Legislation
  • (Definitions, Controlled Ingredients, PIP, Labelling/PAO,
  • Perfumes/Allergens)
  • Questions & Answers session
  • Lunch (provided)
  • Process of Cosmetic Safety Assessment (Risk Hazard, Exposure, Toxicological Risk Assesments, Assessors Role,Assessment Process, human trials)
  • Questions & Answers session

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to see how Intertek can help your organization with Cosmetics Safety Seminar.