Informed consent in toxicology should cover several key components:
Purpose of the Study: Clear explanation of the study’s objectives. Procedures: Detailed description of what the participant will undergo. Risks and Benefits: Comprehensive outline of potential risks and expected benefits. Alternatives: Information on any alternative procedures or treatments available. Confidentiality: Assurance on how personal data will be protected. Voluntary Participation: Statement that participation is voluntary and participants can withdraw at any time without penalty.
