European Union · Question · QUESTION_WRITTEN
E-9-2020-005219
Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)
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24 September 2020
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answered
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Discovery layer
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27 November 2020
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1 official language
Dutch
Tenuitvoerlegging van de nieuwe verordening betreffende medische hulpmiddelen voor in-vitrodiagnostiek (Verordening (EU) 2017/746)
Records
Official question E-9-2020-005219 from European Union at European Parliament. Dated 24 September 2020. Status: answered.
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7 official files
Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)
QUESTION_WRITTEN · EN · 9 October 2020
Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)
QUESTION_WRITTEN · EN · 9 October 2020
Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)
QUESTION_WRITTEN · EN · 9 October 2020
Answer
QUESTION_WRITTEN_ANSWER · 27 November 2020
Tenuitvoerlegging van de nieuwe verordening betreffende medische hulpmiddelen voor in-vitrodiagnostiek (Verordening (EU) 2017/746)
QUESTION_WRITTEN · NL · 9 October 2020
Tenuitvoerlegging van de nieuwe verordening betreffende medische hulpmiddelen voor in-vitrodiagnostiek (Verordening (EU) 2017/746)
QUESTION_WRITTEN · NL · 9 October 2020
Tenuitvoerlegging van de nieuwe verordening betreffende medische hulpmiddelen voor in-vitrodiagnostiek (Verordening (EU) 2017/746)
QUESTION_WRITTEN · NL · 9 October 2020
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