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Advocacy group urges swift implementation of procurement process to benefit patients Cure SMA Foundation of India, a parent-led patient advocacy organisation for Spinal Muscular Atrophy (SMA), has commended recent steps taken by the Government of India, the judiciary, and healthcare stakeholders to address rare diseases. The Ministry of Health and Family Welfare and the Delhi High Court have allocated over Rs 900 crore for rare disease treatment, including SMA, marking a milestone for the com ...Read More >
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