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The complete approval process consists of five major stages: preclinical toxicology studies, Phase I human safety and tolerance testing, Phase II efficacy evaluation, Phase III large-scale controlled clinical trials, and GMP manufacturing site audits

As fitting function, the following equation was used where M z (t) is the longitudinal relaxation at the recovery delay time t , M 0 is the equilibrium magnetization and R i is either the longitudinal relaxation rate R 1 or R 1

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We have streamlined DSIP therapy to make it simple and effective