A whitelist does not imply 20 years testing data. It means, allowed substances need to be explicitly authorized before introduction to the consumer market. For

A whitelist does not imply 20 years testing data. It means, allowed substances need to be explicitly authorized before introduction to the consumer market. For food, pharmacological and cosmetic ingredients, the EFSA requires scientific evaluation concluding no harmful effects in advance. Of course, if later harmful effects are observed authorization can be withdrawn. This is in contrast to e.g. the FDA process where such substances do not have to be demonstrated safe like that beforehand, AFAIK. https://food.ec.europa.eu/safety/chemical-safety_en https://food.ec.europa.eu/safety/chemical-safety_en https://environment.ec.europa.eu/strategy/chemicals-strategy_en https://environment.ec.europa.eu/strategy/chemicals-strategy...