MARTINOVSKÝ Aleš

5 declared company affiliations

Source: EUDAMED

Public regulatory data · synced 2026-08-05

20%

MARTINOVSKÝ Aleš is a Person Responsible for Regulatory Compliance (PRRC) in the medical device industry. Currently affiliated with BIOMAG. 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 →
Regulatory Compliance
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 →
The conformity of the MDs is appropriately checked, in accordance with the QMS under which the MDs are manufactured, before an MD is released; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the PMS obligations are complied with in accordance with Art.10(10) MDR; the reporting obligations referred to in Art.87–91 MDR are fulfilled; in the case of investigational MDs, the statement referred to in Section 4.1 of Annex XV 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 →
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 →
The conformity of the MDs is appropriately checked, in accordance with the QMS under which the MDs are manufactured, before an MD is released; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the PMS obligations are complied with in accordance with Art.10(10) MDR; the reporting obligations referred to in Art.87–91 MDR are fulfilled; in the case of investigational MDs, the statement referred to in Section 4.1 of Annex XV MDR is issued.

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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 →
Regulatory Compliance
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 →
The conformity of the MDs is appropriately checked, in accordance with the QMS under which the MDs are manufactured, before an MD is released; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the PMS obligations are complied with in accordance with Art.10(10) MDR; the reporting obligations referred to in Art.87–91 MDR are fulfilled; in the case of investigational MDs, the statement referred to in Section 4.1 of Annex XV 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 →
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 →
The conformity of the MDs is appropriately checked, in accordance with the QMS under which the MDs are manufactured, before an MD is released; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the PMS obligations are complied with in accordance with Art.10(10) MDR; the reporting obligations referred to in Art.87–91 MDR are fulfilled; in the case of investigational MDs, the statement referred to in Section 4.1 of Annex XV MDR is issued.

MARTINOVSKÝ Aleš

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