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356, 360e-3) to non-addictive medical products intended to treat pain or addiction, including the circumstances under which the Secretary- (A)may apply the eligibility criteria under such sections 506 and 515B to non-opioid or non-addictive medical products intended to treat pain or addiction; (B)considers the risk of addiction of controlled substances approved to treat pain when establishing unmet medical need; and (C)considers pain, pain control, or pain management in assessing whether a disease or condition is a serious or life-threatening disease or condition; (2)the methods by which sponsors may evaluate acute and chronic pain, endpoints for non-addictive medical products intended to treat pain, the manner in which endpoints and evaluations of efficacy will be applied across and within review divisions, taking into consideration the etiology of the underlying disease, and the manner in which sponsors may use surrogate endpoints, intermediate endpoints, and real world evidence; (3)the manner in which the Food and Drug Administration will assess evidence to support the inclusion of opioid sparing data in the labeling of non-addictive medical products intended to treat pain, including- (A)data collection methodologies, including the use of novel clinical trial designs (consistent with section 3021 of the 21st Century Cures Act (Public Law 114-255)), and real world evidence (consistent with section 505F of the Federal Food, Drug, and Cosmetic Act (21 U.S.C

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The Secretary shall maintain a program, to be known as the Minority Fellowship Program, under which the Secretary shall award fellowships, which may include stipends, for the purposes of- (1)increasing the knowledge of mental and substance use disorders practitioners on issues related to prevention, treatment, and recovery support for individuals who are from racial and ethnic minority populations and who have a mental or substance use disorder; (2)improving the quality of mental and substance use disorder prevention and treatment services delivered to racial and ethnic minority populations; and (3)increasing the number of culturally competent mental and substance use disorders professionals who teach, administer services, conduct research, and provide direct mental or substance use disorder services to racial and ethnic minority populations. We offer in the rooms you hot and live camsex in HD, 3D, Cam2Cam with sound and in high quality. The Assistant Secretary shall award grants to eligible entities- (1)to establish assertive community treatment programs for adults with a serious mental illness; or (2)to maintain or expand such programs. Grants under this subsection shall be made to improve- (A)screening children and adolescents for alcohol use; (B)offering brief interventions to children and adolescents to discourage such use; (C)educating parents about the dangers of, and methods of discouraging, such use; (D)diagnosing and m xxx com treating alcohol use disorders; and (E)referring patients, when necessary, to other appropriate care

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Not later than 5 years after the date of the enactment of this Act, the Secretary shall make publicly available on the Internet website of the Food and Drug Administration a report. The working group shall- (A)not later than 2 years after the date of enactment of this Act, develop or update a summary of- (i)ongoing tick-borne disease research, including research related to causes, prevention, treatment, surveillance, diagnosis, diagnostics, duration of illness, and intervention for individuals with tick-borne diseases; (ii)advances made pursuant to such research; (iii)Federal activities related to tick-borne diseases, including- (I)epidemiological activities related to tick-borne diseases; and (II)basic, clinical, and translational tick-borne disease research related to the pathogenesis, prevention, diagnosis, and treatment of tick-borne diseases; (iv)gaps in tick-borne disease research described in clause (iii)(II); (v)the Working Group’s meetings required under paragraph (4); and (vi)the comments received by the Working Group; (B)make recommendations to the Secretary regarding any appropriate changes or improvements to such activities and research; and (C)solicit input from States, localities, and nongovernmental entities, including organizations representing patients, health care providers, researchers, and industry regarding scientific advances, research questions, surveillance activities, and emerging strains in species of pathogenic organi