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The NIH Clinical Trial Integrity Act requires NIH-funded research organizations to establish clear, measurable goals for recruiting and retaining diverse clinical trial participants across race, ethnicity, age, and sex categories that reflect the disease prevalence or general U.S. population. The bill mandates detailed recruitment and retention plans, requires annual reporting of demographic data, and directs researchers to complete diversity training. It also authorizes a study on modernizing regulations for participant compensation and reimbursement, and establishes a national public awareness campaign with grants to community organizations to increase clinical trial participation among underrepresented populations.
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