4. In vitro diagnostic medical devices ***I - Medical devices ***I (debate)

Verbatim reports

Report on the proposal for a regulation of the European Parliament and of the Council on in vitro diagnostic medical devices [COM(2012)0541 - C7-0317/2012- 2012/0267(COD)] - Committee on the Environment, Public Health and Food Safety. Rapporteur: Peter Liese (A7-0327/2013)

Report on the proposal for a regulation of the European Parliament and of the Council on medical devices, and amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 [COM(2012)0542 - C7-0318/2012- 2012/0266(COD)] - Committee on the Environment, Public Health and Food Safety. Rapporteur: Dagmar Roth-Behrendt (A7-0324/2013)

Dagmar Roth-Behrendt and Peter Liese presented their reports.

The following spoke: Neven Mimica (Member of the Commission).

The following spoke: Edite Estrela (rapporteur for the opinion of the EMPL Committee), Nora Berra (rapporteur for the opinion of the IMCO Committee), Mairead McGuinness, on behalf of the PPE Group, Gilles Pargneaux, on behalf of the S&D Group, Rebecca Taylor, on behalf of the ALDE Group, Margrete Auken, on behalf of the Verts/ALE Group, Alda Sousa, on behalf of the GUE/NGL Group, Derek Roland Clark, on behalf of the EFD Group, Jolanta Emilia Hibner, Christel Schaldemose, who also replied to a blue-card question by Margrete Auken, Holger Krahmer, Michèle Rivasi, Richard Seeber, Andrés Perelló Rodríguez, Milan Cabrnoch, Zofija Mazej Kukovič, Françoise Grossetête and Thomas Ulmer.

The following spoke under the 'catch-the-eye' procedure: Danuta Jazłowiecka, Spyros Danellis, Petru Constantin Luhan, Biljana Borzan, Phil Prendergast and Antigoni Papadopoulou.

The following spoke: Neven Mimica, Dagmar Roth-Behrendt and Peter Liese.

The debate closed.

Vote: minutes of 22.10.2013, item 6.3 and minutes of 22.10.2013, item 6.4.