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Summary of Workshop on Use of Data Developed during Drug Development for Read across to Environmental Analyses

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References

  1. Committee for Medicinal Products for Human Use (CHMP). Guideline on the Environmental Risk Assessment of Medicinal Products for Human Use. EMEA/CHMP/SWP/4447/00. Available at: http://www.emea.europe.eu/int/pdfs/human/swp/444700en.pdf. Accessed January 20, 2007.

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Authors and Affiliations

  1. Federal Institute for Drugs and Medical Devices, Germany

    Klaus Olejniczak

  2. Pfizer, USA

    Richard T. Williams

  3. Medical Products Agency, Sweden

    Thomas Kühler

  4. BioLogue, University of Copenhagen, Blegdamsvej 3A, DK-2200, Copenhagen N, Denmark

    Per Spindler DVM, MSc, EMBA (Director)

Authors
  1. Klaus Olejniczak
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  2. Richard T. Williams
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  3. Thomas Kühler
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  4. Per Spindler DVM, MSc, EMBA
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Corresponding author

Correspondence to Per Spindler DVM, MSc, EMBA.

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Olejniczak, K., Williams, R.T., Kühler, T. et al. Summary of Workshop on Use of Data Developed during Drug Development for Read across to Environmental Analyses. Ther Innov Regul Sci 41, 201–202 (2007). https://doi.org/10.1177/009286150704100212

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  • DOI: https://doi.org/10.1177/009286150704100212

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