Helpline
+91 8892 555 000
Email : contactus@ordindia.in

Vision, Mission & Objectives

ORDI (www.ordindia.in) is a national umbrella organization representing the collective voice of all patients with rare diseases in India, setup as a section 25 non-profit company in India.
Vision:
 A Better Life for people with Rare Diseases.
Mission:
ORDI’s mission is to be the strong united voice for all rare diseases in India, to reduce inequalities and ensure that people living with rare diseases have access to the same resources as any other population
Objectives:
  1. To promote Rare Diseases as human rights priority through public awareness.
  2. To contribute towards development of Public Policy and take part in implementation, such as Rare Disease Policy and Orphan Drug Policy.
  3. To collaborate with advocacy organizations from India, and people living with rare diseases; working jointly  to connect them with national & international forums such as  NORD, EURORDIS, RDI, Global gene, UDN,  etc.
  4. To accelerate diagnosis and treatment options for patients with rare diseases through public-private partnerships, and by advocating mandatory New Born screening·
  5. To Facilitate & encourage Clinical Trials , Research & Orphan drug development activities.
Upcoming Events

Our Executive Director Mr. Prasanna Shirol was a part of First Ever summit dedicated to advancing equitable care for rare diseases in older adults. The meeting was attended from 25 countries across Canada, Latin America, Europe, and Asia, representing patient and caregiver communities, patient advocates, healthcare professionals, and healthcare policy experts. This is a short video highlighting the impact of the initiative to date, in the words of the COLLABORATE Community.

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