TELES Liliana

4 declared company affiliations

Source: EUDAMED

Public regulatory data · synced 2026-08-22

20%

TELES Liliana is a Person Responsible for Regulatory Compliance (PRRC) in the medical device industry. Currently affiliated with DAVID MEDICAL EUROPE, UNIPESSOAL LDA. Explore their full professional profile and affiliations on MD Atlas.

UnclaimedBuilt automatically from EUDAMED

Is this you? Claim this page — free

Verify your identity to edit your headline, publish your own contact details and control how you appear across MD Atlas. Takes under two minutes. No card required.

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 conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; 2. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 3. Compliance with post-market surveillance obligations and incident reporting obligations 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 conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; 2. The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 3. Compliance with post-market surveillance obligations and incident reporting obligations 4. In the case of investigational devices, ensure 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 →
Obligations under MDR Article 15(3).
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 →
Responsibilities under point 3 of Article 15 to the Regulation (EU) 2017/746.
Source: EUDAMED · non-removable

Unlocks when claimed + on QARA

Join the QARA community

Coming soon

We're building a private network for quality & regulatory affairs professionals. Be the first to know when it opens.

By subscribing you accept the Privacy Policy.

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 conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; 2. the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 3. Compliance with post-market surveillance obligations and incident reporting obligations 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 conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; 2. The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 3. Compliance with post-market surveillance obligations and incident reporting obligations 4. In the case of investigational devices, ensure 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 →
Obligations under MDR Article 15(3).
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 →
Responsibilities under point 3 of Article 15 to the Regulation (EU) 2017/746.
Source: EUDAMED · non-removable

TELES Liliana

Is this you? Claim this page — free

Company affiliations

Join the QARA community

Is this you? Claim this page — free

Company affiliations

About & headline

Services & frameworks

Availability & hire