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HERKA Katarzyna

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 →

4 declared company affiliations

Source: EUDAMED

Public regulatory data · synced 2026-06-19

20%

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

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Company affiliations

  • .

    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 →
    1/ sprawdzanie zgodności wyrobów z systemem zarządzania jakością przed zwolnieniem ich do obrotu, 2/ sporządzanie i aktualizacja dokumentacji technicznej i deklaracji zgodności UE, 3/ zapewnienie przestrzegania obowiązków nadzoru po wprowadzeniu do obrotu,
    Source: EUDAMED · non-removable
  • "RAKO OPTYK SERWIS" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

    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 →
    Artykuł 15 ust. 3 Rozporządzenia UE 2017/745, punkty a, b, c, d, e (w całości i bez wykluczeń).
    Source: EUDAMED · non-removable
  • KIKGEL Sp. z o.o.

    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
  • OKO Optical

    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 →
    Zakres na podstawie Artykułu 15 ust. 3 (a, b, c, d, e) Rozporządzenia Parlamentu Europejskiego i Rady (UE) 2017/745 z dnia 5 kwietnia 2017 r. w sprawie wyrobów medycznych - bez wykluczeń i w pełnym zakresie.
    Source: EUDAMED · non-removable
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