Any manufacturer who places substances or preparations on the market shall be responsible for ensuring that they do not endanger life or health. In particular, the manufacturer shall:
assess and classify substances and preparations according to their properties;
package and label them in accordance with the type of hazard concerned.
The Federal Council shall issue regulations on the nature, extent and review of self-regulation. In particular, it shall specify:
test methods, the principles of Good Laboratory Practice (GLP) and the criteria for assessment and classification;
packaging and labelling requirements.
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