On the occasion of Rare Disease Day on 28 Feb, Bengaluru-based Strand ...
Dr Meenakshi Bhat, a pioneering clinical geneticist at the Centre for ...
AstraZeneca Pharma India has announced a Central Drugs Standard Contro...
To address the rare disease burden in India, Bengaluru-based MedG...
The Central Drugs Standard Control Organisation (CDSCO) stated recentl...
Governments across the world have regulatory incentives to support orp...
With the third consecutive term win of the government, rare disease pa...
What has it been like to raise awareness about rare diseases among pat...
The Organisation for Rare Diseases India (ORDI), a decade old non-prof...
The scientific community has a critical role to play in accelerating r...
Patients diagnosed with Acid Sphingomyelinase Deficiency (...
The Central Government has given full exemption from basic custom...
AstraZeneca India has announced its entry into rare disease therapy in...
Bengaluru-based MedGenome Labs has announced the launch of a ...
The death of a 13-year-old Ghaziabad boy suffering from Hunter Syndrom...
To tackle any disease requires sustained research and development (R&a...
Sanofi Speciality Care has reaffirmed its commitment to rare diseases ...
The Karnataka government has launched a research and training unit for...
