On World Rare Diseases Day, India’s focus is on the high cost of treatments for rare diseases due to monopoly drug pricing. The National Policy for Rare Diseases aims to lower costs and promote local drug manufacturing. A patient’s court battle for affordable SMA treatment highlights the need for policy implementation and transparent drug pricing. Post navigation Watch: EU chief Ursula von der Leyen witnesses UPI payment system for first time in India, says ‘bravo’ Himachal government asks temples for donations, BJP says ‘attack on Sanatan Dharma’