+Article 10 3

Article 10 3

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.

1. Przegląd

,

1.1 Odwołania

1.2 Zidentyfikowane wymagania

1.3 Powiązane normy

2. Zidentyfikowane wymagania

Wymagania

3. Powiązane normy

Normy