The Minister of Science and Technology launched 'BIRSA 101', India's first indigenous CRISPR-based gene therapy for Sickle Cell Disease. Named after Birsa Munda on his 150th birth anniversary, the therapy was developed by CSIR-IGIB (Institute of Genomics and Integrative Biology) and transferred to the Serum Institute of India.

The CRISPR-Cas9 technology works like molecular scissors to cut DNA at specific target sites, correcting the HBB gene mutation that causes sickle cell disease. Global gene therapies cost ₹20-25 crore, but BIRSA 101 aims to be affordable. This supports the National Sickle Cell Anaemia Elimination Mission (2023-2047). Rajasthan's tribal populations in southern districts like Banswara and Dungarpur have significant sickle cell prevalence.