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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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National award for role model with disability

BANGALORE: Rajdeep Manwani’s Economics classes are famous. There is a little bit of history, conversation and lots of stories seasoned with wit. It is a class that no student would...

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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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Initiative to make rare diseases diagnosable

In an effort to make rare diseases diagnosable and curable. In an effort to make rare diseases diagnosable and curable an initiative Organisation for Rare Diseases India(ORDI) was lanuched by...

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