HRPP stands for Human Research Protection Program. It is a comprehensive framework comprising policies, procedures, and guidelines designed to safeguard the rights, welfare, and wellbeing of individuals participating in research studies or clinical trials involving human subjects. The primary goal of HRPP is to ensure that research involving human subjects is conducted ethically, responsibly, and in compliance with applicable regulations, laws, and institutional policies.
The HRPP is implemented by research institutions, such as universities or healthcare organizations, to establish the necessary infrastructure for protecting human subjects. This program typically includes several components, such as an institutional review board (IRB) responsible for reviewing and approving research protocols, a research compliance office to enforce regulations and policies, and a data and safety monitoring board to ensure ongoing monitoring and evaluation of research activities.
The HRPP plays a critical role in promoting the ethical conduct of research involving human subjects. It mandates adherence to key ethical principles, including respect for autonomy, beneficence, and justice. It requires thorough review of research protocols to ensure that risks are minimized, potential benefits are maximized, and the informed consent process is adequately implemented. The HRPP also has provisions for ongoing monitoring of research activities to detect and promptly address any potential risks or violations.
Overall, the HRPP serves as a crucial mechanism for protecting the rights and welfare of individuals participating in research studies, while also maintaining high ethical standards and compliance with legal and regulatory requirements.
