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The Delhi High Court has extended the tenure of the National Rare Disease Committee (NRDC) for 5 years, empowering it with a broader mandate to strengthen rare disease management in India.

NRDC Extended for Five Years to Boost Rare Disease Initiatives

By IORD | 0 comment
Delhi: In a significant decision, the Delhi High Court has extended the tenure of the National Rare Disease Committee (NRDC) and broadened its mandate. This move aims to establish a more coordinated,
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In a landmark ruling, the Delhi High Court ordered the creation of a ₹974 crore National Fund for Rare Diseases for 2024–26, emphasizing patient-centric policies, expanded treatment access, and funding reforms.

National Fund for Rare Diseases Announced: ₹974 Crore Allocated for 2024–26

By IORD | 0 comment
Delhi: In a set of pathbreaking directions that is set to help the rare disease fraternity in India, the Delhi High Court has directed the Union of India to establish the National Fund for Rare Diseas
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The Delhi High Court has introduced a landmark Standard Protocol to streamline rare disease management, ensuring continuous availability of therapies, local drug manufacturing, and time-bound treatment delivery.

Delhi High Court Sets Up Standard Protocol for Rare Disease Treatment

By IORD | 0 comment
Delhi: In a landmark judgment, the Delhi High Court ordered the setting up of a comprehensive Standard Protocol for managing rare disease cases at Centers of Excellence (CoEs). The protocol mandates c
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IORD & Rare Diseases in India: Impact, Initiatives & Challenges

IORD & Rare Diseases in India: Impact, Initiatives & Challenges

By IORD | 0 comment
Rare diseases, though affecting a small percentage of the population, represent a significant public health challenge in India. The Indian Organisation for Rare Diseases (IORD) has been at the forefro
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IORD Webinar on Global Burden of Rare Diseases: Issues and Challenges

Registration Open for Webinar on Global Burden of Rare Diseases: Issues and Challenges

By IORD | 0 comment
Join an expert-led webinar exploring the complexities of rare diseases, featuring insights from IORD CEO & President Prof. Ramaiah MuthyalaRare diseases are a pressing global health issue, with an
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Indian Organisation for Rare Diseases represented India at Rare Diseases International (RDI) Membership Meeting held on October 21-22, 2024, in Barcelona, Spain.

IORD Champions Rare Disease Advocacy at RDI Meeting in Barcelona

By IORD | 0 comment
The following excerpt is  from a presentation delivered by Krishnaji Rao Muthyala, Secretary of the Indian Organization for Rare Diseases (IORD), at the Rare Diseases International (RDI) Membership Me
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IORD

Indian Organization For Rare Diseases (IORD), a not-for-profit umbrella organization represents interests of all stakeholders of Rare Diseases in India including individual patients, patient support groups, health policy advocates and health care providers.

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Indian Organization For Rare Diseases
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Phone: +91-9666438880

Email: indiaord@gmail.com

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  • Home
  • About Us
    • Management Committee
    • Advisory Board
    • Newsletters
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  • Rare Diseases
  • Research
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  • Gallery
    • Photo Gallery
      • World Rare Disease Day – 2023
      • World Rare Disease Day 2020
    • Video Gallery
      • World Rare Disease Day – 2020
      • World Rare Disease Day – 2019
      • World Rare Disease Day – 2018
  • Blog
  • Contact Us
IORD – Indian Organization for Rare Diseases