Topic outline

  • General

    • Gerpac Europharmat Medical Devices Guide

      These recommendations concern medical devices intended for the preparation and parenteral administration
      of cytotoxic medications and, by extension, any drug involving risks for staff and the environment.

      Some pharmaceutical specialities including a technical solution allowing preparation and/or administration to be optimised may also be concerned by these recommendations.

      They do not concern collective and individual protection equipment used for such applications.
      These recommendations do not constitute Good Preparation Practices. The reader should refer to the applicable issue of Good Preparation Practices provided in articles L.5121-5 and R.5126-14.

      The GERPAC – EUROPHARMAT working group

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