RECENT ADVANCES IN ETHICAL CONSIDERATIONS AND INFORMED CONSENT IN CLINICAL TRIAL

Sandeep Mewada*, Bivek Sharma and Fameen Shaik

ABSTRACT

In recent years, significant advances in ethical considerations and informed consent practices in clinical trial have emerged to safeguard the rights and well-being of study participants. Improved informed consent processes now offer clear and understandable information to participants using multimedia tools and simplified language. Digital informed consent through electronic platforms streamlines the process and captures electronic signatures. Researchers adopt participant-centric approaches, incorporating their perspectives and preferences in trial design and consent documents. Special focus on ethical considerations for vulnerable populations ensures additional safeguards for their protection. Data privacy and security measures address concerns about personal information. The risk of real-world evidence and practical trials promotes research relevance while maintaining ethical standards. Continuous ethics oversight and global collaboration aim to harmonize ethical guidelines and temporary responsible and ethical clinical research. These advancements collectively reinforce the commitment to uphold ethical standards and prioritize participant welfare throughout the clinical trial process.

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