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Journal of Bioethical Inquiry

, Volume 6, Issue 1, pp 141–143 | Cite as

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  • Diana M BowmanEmail author
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The Therapeutic Goods Administration (TGA) is charged with the responsibility of safeguarding public health by ensuring the quality, safety, efficacy and timely availability of therapeutic goods within Australia. This is achieved through a combination of manufacturing principles, pre-market risk assessments and post-market monitoring processes. Sunscreen products with a SPF factor of 4 or above are defined as a therapeutic good (TGA 2003), and therefore fall within the regulatory scope of the TGA. The majority of these sunscreen products are defined as “listable goods”, and assessed by the TGA on the basis of their quality and safety; they are therefore not required to assess the efficacy of the sunscreen prior to its listing, and rely instead on the scientific evidence supplied by the applicant. Prime facie, it is therefore possible to assume that all current sunscreens that fall under the regulatory scope of the TGA—regardless of whether or not they contain nanoparticles—are safe...

Keywords

Zinc Oxide Nanoscale Material Therapeutic Good Administration Therapeutic Good Viable Epidermis 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media B.V. 2008

Authors and Affiliations

  1. 1.Monash Centre for Regulatory Studies, Faculty of LawMonash UniversityClaytonAustralia
  2. 2.Institute for Environment and Energy Law, Faculty of LawKU LeuvenLeuvenBelgium

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