Article 6 5

(a)

assessing the impact of chemicals on human health and the environment;

(b)

monitoring time and spatial trends in exposure;

(c)

developing health risk and impact indicators;

(d)

monitoring the impact of regulatory intervention;

(e)

performing regulatory risk assessment and regulatory risk management;

(f)

in the context of studies under the data generation mechanism referred to in Article 24 and the human biomonitoring study referred to in Article 25;

(g)

assessing the need for regulatory action and prioritising such action;

(h)

supporting policy making and the development of legislation, including by carrying out scientific research to that effect;

(i)

facilitating the processing of human biomonitoring data by the Commission, the EEA, the EFSA, the EMA, and EU-OSHA in accordance with paragraphs 3, 4, 6 and 7.