(21)Although the information yielded on substances through evaluation should be used in the first place by manufacturers and importers to manage the risks related to their substances, it may also be used to initiate the authorisation or restrictions procedures under this Regulation or risk management procedures under other Community legislation. Therefore it should be ensured that this information is available to the competent authorities and may be used by them for the purpose of such procedures.
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New version applies from 01/12/2010.
74 provisions change.
Later versions: 21/02/2011, 06/03/2011, 05/05/2011, 10/12/2011, 01/06/2012, 05/06/2012, 09/10/2012, 06/03/2013, 21/04/2013, 01/07/2013, 10/04/2014, 22/08/2014, 01/01/2015, 23/03/2015, 13/05/2015, 01/06/2015, 25/09/2015, 27/12/2015, 03/02/2016, 08/03/2016, 01/04/2016, 21/06/2016, 14/07/2016, 11/10/2016, 02/01/2017, 02/03/2017, 04/07/2017, 10/10/2017, 31/01/2018, 01/03/2018, 09/05/2018, 01/12/2018, 07/01/2019, 02/07/2019, 30/10/2019, 01/01/2020, 27/02/2020, 28/04/2020, 24/08/2020, 01/01/2021, 15/02/2021, 05/07/2021, 25/08/2021, 01/10/2021, 08/01/2022, 01/03/2022, 01/05/2022, 14/10/2022, 17/12/2022, 28/05/2023, 29/06/2023, 06/08/2023, 01/12/2023, 06/06/2024, 10/10/2024, 22/04/2025, 23/06/2025, 01/09/2025, 23/10/2025, 11/05/2026, 22/06/2026.
Recital 21 changes in this version: compare with the current text.