Risikooplysninger

Risikooplysninger refers to information that describes the hazards and the level of risk associated with a product, process, or activity, and the measures needed to control those risks. They are used for risk assessment, decision-making, and risk communication among stakeholders, with the aim of preventing harm and promoting safety.

The scope of Risikooplysninger is broad and applies across many sectors. In workplace safety, it includes hazard identifications, exposure scenarios, risk assessments, and recommended protective measures. For chemical handling and consumer products, it encompasses labeling, safety data sheets, and instructions that communicate how to handle, store, and dispose of substances safely. In healthcare, risk information is part of pharmacovigilance and risk management plans that describe potential adverse effects and strategies to minimise risk.

Regulatory frameworks that govern Risikooplysninger vary by jurisdiction but share common elements. In the European Union, regulations such as REACH and CLP require hazard classifications and safety information for chemicals, while Safety Data Sheets provide structured risk information. Occupational safety legislation requires employers to assess risks and communicate them to workers. In the pharmaceutical sector, risk management plans and pharmacovigilance activities provide formal risk information about medicines.

Production and dissemination of Risikooplysninger involve collecting data from testing, monitoring, and incident reporting, and compiling it into accessible documents and channels. Common formats include safety data sheets, product labels, risk assessments, standard operating procedures, and training materials. Accessibility, accuracy, and timely updates are essential to ensure effective risk communication to all stakeholders, including employers, employees, patients, and regulators.