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.
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- OGH Makes History with Rare Liver Transplant
- RJS PBH Webinar: Prof. Ramaiah Muthyala’s Keynote on World Health Day 2025
- World Rare Disease Day 2025: IORD Advocates for Policy & Awareness
- Prof Ramaiah Muthyala: A Call for Policy Change and Rare Disease Healthcare in Andhra Pradesh
- Undiagnosed Disease Network Conference – Congenital Ichthyosis Case Study from India
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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.
CONTACT US
Indian Organization For Rare Diseases
Reg. Office (India): Plot 397, Road 22b, Jubilee Hills, Hyderabad (Telangana) 500033, Telangana, India
Phone: +91-9666438880
Email: indiaord@gmail.com