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Minutes
Monday, 25 March 2019 - Strasbourg

7. Corrigenda (Rule 231)

The ENVI Committee had submitted the following corrigenda to texts adopted by Parliament:

—   Corrigendum P8_TA(2017)0107(COR01) to Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (OJ L 117, 5.5.2017, p. 1-175) - (position of the European Parliament adopted at second reading on 5 April 2017 with a view to the adoption of the above regulation P8_TA(2017)0107) - (10728/4/2016 – C8-0104/2017 – 2012/0266(COD))

—   Corrigendum P8_TA(2017)0108(COR01) to Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (OJ L 117, 5.5.2017, p. 176-332) - (position of the European Parliament adopted at second reading on 5 April 2017 with a view to the adoption of the above regulation P8_TA(2017)0108) - (10729/4/2016 – C8-0105/2017 – 2012/0267(COD)).

The corrigenda were available on Europarl.

Pursuant to Rule 231(4), these corrigenda would be deemed approved unless, within 24 hours, a request was made by a political group or a number of Members reaching at least the low threshold that they be put to the vote.

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