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.