ORD India – Be Aware And Preventive
ORD India. Welcome to ORD...
Read Ordindia.org news digest here: view the latest ORD India articles and content updates right away or get to their most visited pages. Ordindia.org is not yet rated by Alexa and its traffic estimate is unavailable. It seems that ORD India content is notably popular in India. We haven’t detected security issues or inappropriate content on Ordindia.org and thus you can safely use it. Ordindia.org is hosted with CloudFlare, Inc. (United States) and its basic language is English.
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Organization For Rare Diseases India | ORDI
ORDI was founded to address the many challenges in the management of rare disease in India. A lack of awareness about rare disease even among doctors means that
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Harsha K Rajasimha, Ph.D. Dr. Harsha Karur Rajasimha is a genomics scientist, social entrepreneur and co-founder of the Organization for Rare Diseases
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Dr. K. M. Girisha MBBS, DCH, MD, DM Associate Professor, Dept of Paediatrics, KMC, Manipal, from 25.8.2008 till date. Assistant Professor, Sanjay Gandhi
Ordindia.org news digest
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5 years
A rare-disease entrepreneur follows an unconventional drug development path
In 2012, Ethan Perlstein challenged the academic status quo. Now as CEO of the start-up Perlara, can he do the same for the biotech industry?
In 2012, molecular biologist Ethan Perlstein very publicly stepped off the academic treadmill. In his view, the system was raising more young researchers than it could absorb, driving people into an increasingly long training cycle. Perlstein, at the... -
5 years
A comparative study of orphan drugs in US, EU & India
Today, more than 5,000 diseases are catalogued as “rare” by the scientific community, so long as they affect small sections of population. The drugs used for the treatment of rare diseases are known as orphan drugs. An orphan drug is a pharmaceutical...
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5 years
Experts raise concern over delay in implementation of rare diseases treatment po...
Health experts Wednesday highlighted the need for an immediate call-to-action for the implementation of the National Policy for Treatment of Rare Diseases, stating that the patients were suffering and losing out on time.
The policy was approved by the Union Health Ministry in May last year, but it is yet to see light of the day.... -
5 years
After new rare diseases policy, govt incentives needed for finding cures
Medical experts say India also needs an orphan drug policy to provide incentives to pharmaceutical companies to innovate and manufacture drugs for rare diseases
https://www.business-standard.com/article/economy-policy/after-new-rare-diseases-policy-govt-incentives-needed-for-finding-cures-117113000229_1.html...
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