MedGenome Labs, a genomics and clinical data driven diagnostics and dr...
Lysosomal Storage Disorders Support Society (LSDSS), a non-profit orga...
Sanofi Genzyme, the specialty care global business unit of Sanofi...
‘Race For 7’, an initiative championed by the Organization...
The Organization For Rare Diseases India (ORDI), a not for profit orga...
On the occasion of Rare Disease Day, Lysosomal Storage Disorders Suppo...
There are about 2, 75,000 infants born with sickle cell anemia every y...
Lending their collective voice to the rare disease community in India,...
Sanofi Genzyme, the specialty care global business unit of Sanofi...
US based Neuromuscular Disease Foundation (NDF) is launching an allian...
Genzyme made an upfront payment to AstraZeneca of $165 million to acqu...
Sanofi and its subsidiary Genzyme have announced that they have entere...
There are close to 7000 known rare diseases today, most of which are p...
The second day of the 15th edition of Bangalore India BIO was dotted w...
Despite medical advancements, rare diseases are still a common occuren...
India is home to an estimated over seventy million patients affected w...
Karnataka government is all set to introduce a policy for rare disease...
The objective was to raise awareness for the 70 million estimated pati...