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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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GUENTLEUR Frédérique

PRRC — Person Responsible for Regulatory Compliance

The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.

View in glossary →

3 declared company affiliations

Source: EUDAMED

Public regulatory data · synced 2026-06-19

20%

GUENTLEUR Frédérique is a Person Responsible for Regulatory Compliance (PRRC) in the medical device industry. Currently affiliated with CLEANIS. Explore their full professional profile and affiliations on MD Atlas.

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Company affiliations

  • CLEANIS

    PRRC — Person Responsible for Regulatory Compliance

    The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.

    View in glossary →
    Faire en sorte que: - La conformité des dispositifs soit correctement respectée, conformément au système de gestion de la qualité dans le cadre duquel les dispositifs concernés sont fabriqués, avant libération d'un dispositif. - Les obligations en matière de surveillance après commercialisation soient remplies conformément à l'article 10, paragraphe 10. - Les obligations en matière de notification visées aux articles 87 à 91 soient remplies.
    Source: EUDAMED · non-removable
  • GIBAUD

    PRRC — Person Responsible for Regulatory Compliance

    The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.

    View in glossary →
    Source: EUDAMED · non-removable
  • Laboratoires INNOTHERA

    PRRC — Person Responsible for Regulatory Compliance

    The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.

    View in glossary →
    Faire en sorte que: - La conformité des dispositifs soit correctement respectée, conformément au système de gestion de la qualité dans le cadre duquel les dispositifs concernés sont fabriqués, avant libération d'un dispositif. - Les obligations en matière de surveillance après commercialisation soient remplies conformément à l'article 10, paragraphe 10. - Les obligations en matière de notification visées aux articles 87 à 91 soient remplies.
    Source: EUDAMED · non-removable
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