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Press Release: World Rare Diseases Day

World Rare Diseases Day: VGBT and ORDI partner in Karnataka Bangalore: Around seventy million patients in India (three to four million in Karnataka) are affected with one of more than...

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26 Feb 2015 – Press coverage

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Most patients get no treatments – Prasanna Shirol

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Vision group working on rare disease policy – TOI report

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Karnataka Vision Group ready with draft of Rare Diseases and Orphan Drugs Development Act

– Nandita Vijay, Bengaluru The Karnataka Vision Group on Biotechnology has now put in place the draft of the Rare Diseases and Orphan Drugs Development Act. Efforts are on to...

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Vision group working on rare disease policy

ORDI founder Members -Dr Vijay Chandru- Chairman & CEO Strand Life Sciences and Prasanna Shirol- Founder Member -ORDI in Bangalore Bio Conference 2015 along with other Speakers Mr Sandeep Sahaney-...

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CENTOGENE to collaborate with Organization of Rare Diseases of India

CENTOGENE is pleased to announce its sponsorship of the Organization of Rare Diseases of India (ORDI). ORDI is a not-for-profit organization founded and advised by key opinion leaders from medicine,...

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World Immunology day – By PIDPWS-ORDI and IAP Bangalore Chapter in Bangalore Medical College on 27.4.14- The Hindu

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Urgently require systematic investment in infrastructure enhancements

The Government of India is in a perfect position to provide direction and support to meet the urgent unmet needs of the 70+ million rare disease patients, says Harsha K...

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Opening Up the Indian Rare Disease Market: An interview with ORD India

We here at Total Orphan Drugs, as part of this months focus on emerging markets for the orphan drug industry, have been speaking to Harsha K Rajasimha of the newly...

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