EANM guideline for the preparation of an Investigational Medicinal Product Dossier (IMPD)

  • Sergio Todde
  • , Albert D. Windhorst
  • , Martin Behe
  • , Guy Bormans
  • , Clemens Decristoforo
  • , Alain Faivre-Chauvet
  • , Valentina Ferrari
  • , Antony D. Gee
  • , Balazs Gulyas
  • , Christer Halldin
  • , Petra Kolenc Peitl
  • , Jacek Koziorowski
  • , Thomas L. Mindt
  • , Martina Sollini
  • , Johnny Vercouillie
  • , James R. Ballinger
  • , Philip H. Elsinga*
  • *Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    36 Citations (Scopus)

    Abstract

    The preparation of an Investigational Medicinal Product Dossier (IMPD) for a radiopharmaceutical to be used in a clinical trial is a challenging proposition for radiopharmaceutical scientists working in small-scale radiopharmacies. In addition to the vast quantity of information to be assembled, the structure of a standard IMPD is not well suited to the special characteristics of radiopharmaceuticals. This guideline aims to take radiopharmaceutical scientists through the practicalities of preparing an IMPD, in particular giving advice where the standard format is not suitable. Examples of generic IMPDs for three classes of radiopharmaceuticals are given: a small molecule, a kit-based diagnostic test and a therapeutic radiopharmaceutical.

    Original languageEnglish
    Pages (from-to)2175-2185
    Number of pages11
    JournalEuropean Journal of Nuclear Medicine and Molecular Imaging
    Volume41
    Issue number11
    DOIs
    Publication statusPublished - Nov-2014

    Keywords

    • Radiopharmaceutical
    • Clinical trial
    • Investigational medicinal product
    • Guideline

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