Subsequent to risk assessment, practices/procedures, assays/tests, biological agents, equipments and working designs and structures are developed to minimize risk; this is termed as risk regulation. It can be either reactive or proactive.
Reactive risk regulation develops gradually in a piecemeal manner, and is designed to prevent the proven adverse effects shown by earlier products/activities.
But proactive risk regulation is developed to avoid potential hazards that are predicted in advance before there is any empirical evidence for such hazards. Assays and trials are, then deigned to evaluate the safety of the product/process in question and to demonstrate the absence of the predicted hazards.
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