WHA 75.8 emphasizes the importance of public, community, and patient engagement in strengthening clinical trials to ensure high-quality evidence for health interventions.The resolution recognizes that involving communities and patients enhances the relevance, acceptability, and ethical grounding of research. It calls for greater efforts to include diverse populations in trial design, implementation, and evaluation, ensuring equitable access and representation. Additionally, it highlights the need for transparent communication and the dissemination of trial outcomes to build trust and promote informed decision-making, ultimately improving the effectiveness and impact of health research globally.
Please Sign in (or Register) to view further.