Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)

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Official question E-9-2020-005219 from European Union at European Parliament. Dated 24 September 2020. Status: answered.

Timeline

1. 24 September 2020

   Written question

   Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)

   Source: QUESTION_WRITTEN

2. 27 November 2020

   Answer

   Source: QUESTION_WRITTEN_ANSWER

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7 official files

• Answer

  QUESTION_WRITTEN_ANSWER · 27 November 2020

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• 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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• 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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• 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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• Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)

  QUESTION_WRITTEN · EN · 9 October 2020

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• Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)

  QUESTION_WRITTEN · EN · 9 October 2020

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  Vertaal document

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• Implementation of the new In Vitro Diagnostics Regulation (IVDR) (EU 2017/746)

  QUESTION_WRITTEN · EN · 9 October 2020

  ViewDownloadOpen at official source

  Leesvertaling

  Vertaal dit document naar jouw taal. PoliticalRepo bewaart geen aparte kopie per EU-taal.

  Vertaal naarNL · DutchDE · GermanFR · FrenchES · SpanishIT · ItalianPL · PolishPT · PortugueseSV · SwedishDA · DanishFI · FinnishEL · GreekCS · CzechHU · HungarianRO · RomanianBG · BulgarianHR · CroatianSK · SlovakSL · SlovenianLT · LithuanianLV · LatvianET · EstonianGA · IrishMT · Maltese

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Sponsors

• Petra DE SUTTER · AUTHOR
• · COM · ADDRESSEE
• · EU_COMMISSION · ADDRESSEE

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