REDDEN Jeanine

4 declared company affiliations

Source: EUDAMED

Public regulatory data · synced 2026-08-05

20%

REDDEN Jeanine is a Person Responsible for Regulatory Compliance (PRRC) in the medical device industry. Currently affiliated with Stryker GmbH. 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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable
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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable
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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable
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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable

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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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable
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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable
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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable
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 →
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV of the EU MDR is issued.
Source: EUDAMED · non-removable

REDDEN Jeanine

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