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Cosmetic Testing Report

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Practical Aspects of Cosmetic Testing
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Abstract

Cosmetic testing on humans is similar to clinical research involving the participation of human subjects and is submitted to the international guidelines for good clinical research practice (GCRP) [9, 15]. GCRP is a set of ethical and scientific principles for designing, conducting, recording and reporting clinical trials involving humans. These principles should consider and generally apply to all types of research on human subjects including investigation of physiological or pathological process, evaluation of new diagnostic or therapeutic approach, safety and efficacy assessment of medicinal and skin care product. The observance of these principles, wherever applicable, ensures the ethical, scientifically sound and accurate conduct of the research.

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References

  1. Alfaro, V., Cullell-Young, M., Tanovic, A.: Abbreviated clinical study reports with investigational medicinal products for human use: current guidelines and recommendations. Croat. Med. J. 48, 871–877 (2007). Available from: http://www.cmj.hr/2007/48/6/18074423.htm. Accessed 14 June 2009

  2. Altman, D.G., Schulz, K.F., Moher, D., et al.: The revised CONSORT statement for reporting randomized trials: explanation and elaboration. Ann. Intern. Med. 134, 663–694 (2001). Available from: www.consort-statement.org/index.aspx?o=1316. Accessed 14 June 2009

    Google Scholar 

  3. Bossuyt, P.M., Reitsma, J.B., Bruns, D.E., et al.: Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative. Clin. Chem. 49(1), 1–6 (2003). Available from: http://www.clinchem.org/cgi/reprint/49/1/1. Accessed 14 June 2009

  4. Colipa.: Colipa Guidelines. Guidelines for the Evaluation of the Efficacy of Cosmetic Products (2008). Available from: http://www.ncv-cosmetica.nl/upload/File/Richtlijnen/20080704Colipa_Guidelines_Efficacy.PDF. Accessed 14 June 2009

  5. Encyclopedia Britannica.: How to Write a Lab or Science Report. Available from: http://corporate.britannica.com/library/home/BSW_Science_Report.pdf. Accessed 14 June 2009

  6. Fathalla, M.F., Fathalla, M.M.F.: A Practical Guide for Health Researchers. WHO Regional Publications Eastern Mediterranean Series 30, Cairo (2004). Available from: http://www.emro.who.int/publications/pdf/healthresearchers_guide.pdf. Accessed 14 June 2009

  7. Highleyman, L.: A guide to clinical trials. Part II: interpreting medical research. BETA. 18(2), 41–47 (2006). Available from: http://www.sfaf.org/files/site1/asset/beta_2006_win_interpreting.pdf. Accessed 14 June 2009

  8. International Committee of Medical Journal Editors.: Uniform Requirements for Manuscripts Submitted to Biomedical Journals: Writing and Editing for Biomedical Publication (2008). Available from: http://www.icmje.org/icmje.pdf. Accessed 14 June 2009

  9. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use.: ICH Harmonised Tripartite Guideline: Guideline for Good Clinical Practice E6(R1) (2002). Available from: http://www.ich.org/LOB/media/MEDIA482.pdf. Accessed 14 June 2009

  10. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use.: ICH Harmonised Tripartite Guideline: Structure and Content of Clinical Study Reports (E3) (1995). Available from: http://www.ich.org/LOB/media/MEDIA479.pdf. Accessed 14 June 2009

  11. Patrias, K.: Citing Medicine: the NLM Style Guide for Authors, Editors, and Publishers. In: Wendling, D.L. (technical editor), 2nd edn. National Library of Medicine, Bethesda, USA [updated 2009] (2007). Available from: http://www.nlm.nih.gov/citingmedicine. Accessed 14 June 2009

  12. U.S. Department of Health and Human Services. Food and Drug Administration. Center for Drug Evaluation and Research (CDER). Center for Biologics Evaluation and Research (CBER).: Guidance for Industry: Submission of Abbreviated Reports and Synopses in Support of Marketing Applications. Rockville, MD: Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (1999). Available from: http://www.bcg-usa.com/regulatory/docs/1999/FDA199909B.pdf. Accessed 14 June 2009

  13. University of Pennsylvania.: Clinical Research Protocol (2009). Available from: http://www.med.upenn.edu/ohr/docs/ProtocolTemp_guidelines.doc. Accessed 14 June 2009

  14. Word-Medex Pty Ltd.: Word-Medex Guide. How to Write Good Manuscripts (2009). Available from: http://www.word-medex.com.au/formatting/manuscript.htm. Accessed 14 June 2009

  15. World Health Organisation.: Handbook for Good Clinical Research Practice (GCP) (2002). Available from: http://www.who.int/medicines/areas/quality_safety/safety_efficacy/gcp1.pdf. Accessed 14 June 2009

  16. World Health Organization.: Recommended Format for a Research Protocol (2009). Available from: http://www.who.int/rpc/research_ethics/format_rp/en/print.html. Accessed 14 June 2009

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Correspondence to Hristo Dobrev .

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© 2011 Springer-Verlag Berlin Heidelberg

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Dobrev, H. (2011). Cosmetic Testing Report. In: Fluhr, J.W. (eds) Practical Aspects of Cosmetic Testing. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-05067-1_12

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  • DOI: https://doi.org/10.1007/978-3-642-05067-1_12

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