Full text 
Procedure : 2018/2790(RSP)
Document stages in plenary
Document selected : O-000085/2018

Texts tabled :

O-000085/2018 (B8-0416/2018)

Debates :

PV 25/10/2018 - 7
CRE 25/10/2018 - 7

Votes :

Texts adopted :

Thursday, 25 October 2018 - Strasbourg

7. Implementation of the Medical devices and In-vitro diagnostic medical devices Regulations (debate)
Verbatim reports

Question for oral answer (O-000085/2018) by Mairead McGuinness, Biljana Borzan, Bolesław G. Piecha, Gesine Meissner, Kateřina Konečná, Margrete Auken, Piernicola Pedicini and Joëlle Mélin, on behalf of the ENVI Committee, to the Commission: Implementation of the Medical Devices and In-Vitro Diagnostic Medical Devices Regulations (B8-0416/2018)

Mairead McGuinness moved the question.

Elżbieta Bieńkowska (Member of the Commission) answered the question.

The following spoke: Biljana Borzan, on behalf of the S&D Group, Gesine Meissner, on behalf of the ALDE Group, Kateřina Konečná, on behalf of the GUE/NGL Group, Biljana Borzan, to make a clarification, Joëlle Mélin, on behalf of the ENF Group, Andreas Schwab, on behalf of the PPE Group, Dobromir Sośnierz, non-attached Member, Stanislav Polčák, who declined a blue-card question from Dobromir Sośnierz, Carlos Zorrinho, Mairead McGuinness, Tiemo Wölken, Soledad Cabezón Ruiz, who also replied to a blue-card question by Gesine Meissner, and Michèle Rivasi.

The following spoke under the catch-the-eye procedure: Maria Grapini, Notis Marias and Julie Ward.

The following spoke: Elżbieta Bieńkowska.

The debate closed.

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