Article 10 — Information on regulatory processes on chemicals

1. The ECHA shall establish and manage, as part of the common data platform, a new database containing information on regulatory processes and activities on individual chemicals or groups of chemicals that are planned, ongoing or have been completed since the entry into force of this Regulation by the Member States, the national agencies or the Union institutions, the ECHA, the EEA, the EFSA, EU-OSHA or committees referred to in the Union legal acts listed in Annex III. 2. Where competent authorities of the Member States as referred to in any of the Union legal acts listed in Annex III hold information as referred to in paragraph 1, they shall make that information available to the Union agency responsible under the respective Union legal act listed in Annex III without delay. For each regulatory process or activity, at least the following information shall be included: (a) the chemical identity; (b) the Union legal act and the regulatory process in the context of which the activity takes place; (c) the person or body responsible for the regulatory process or activity; (d) the status of the regulatory process or activity; (e) the outcome of the regulatory process or activity, including, where applicable, any reports or opinions adopted; (f) where applicable, the intended start date of the regulatory process or activity, and the date of completion and latest progress update. 3. Where the ECHA, the EEA, the EFSA, EU-OSHA or the Commission hold information as referred to in paragraph 1, they shall make that information available to the ECHA for incorporation in the common data platform in the standard formats provided for in Article 17 without delay and, where relevant, once the agency responsible or the Commission has carried out a validity assessment. When making that information available, at least the following information shall be included for each regulatory process or activity: (a) the chemical identity; (b) the Union legal act and the regulatory process in the context of which the activity takes place; (c) the person or body responsible for the regulatory process or activity; (d) the status of the regulatory process or activity; (e) the outcome of the regulatory process or activity, including, where applicable, any reports or opinions adopted; (f) where applicable, the intended start date of the regulatory process or activity, and the date of completion and latest progress update. 4. The information referred to in paragraph 3, points (a) to (f), on a specific regulatory process or activity shall be made available to the public once that process or activity has formally started.