LIN Yolanda

4 declared company affiliations

Source: EUDAMED

Public regulatory data · synced 2026-06-21

20%

LIN Yolanda is a Person Responsible for Regulatory Compliance (PRRC) in the medical device industry. Currently affiliated with GMC Inc.. 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. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date 2. the post-market surveillance obligations are complied with in accordance with Article 10(10) 3. the reporting obligations referred to in Articles 87 to 91 are fulfilled 4. in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV 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 →
1. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date 2. the post-market surveillance obligations are complied with in accordance with Article 10(10) 3. the reporting obligations referred to in Articles 87 to 91 are fulfilled 4. in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV 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 →
1. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date 2. the post-market surveillance obligations are complied with in accordance with Article 10(10) 3. the reporting obligations referred to in Articles 87 to 91 are fulfilled 4. in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV 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

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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. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date 2. the post-market surveillance obligations are complied with in accordance with Article 10(10) 3. the reporting obligations referred to in Articles 87 to 91 are fulfilled 4. in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV 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 →
1. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date 2. the post-market surveillance obligations are complied with in accordance with Article 10(10) 3. the reporting obligations referred to in Articles 87 to 91 are fulfilled 4. in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV 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 →
1. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date 2. the post-market surveillance obligations are complied with in accordance with Article 10(10) 3. the reporting obligations referred to in Articles 87 to 91 are fulfilled 4. in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV 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

LIN Yolanda

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