Rare diseases are medical conditions that affect a small percentage of the population. They often go undiagnosed for years. Many are genetic in nature. Treatment options can be limited and expensive. Awareness is crucial for research funding. Support networks help patients and families. Governments and organisations work to improve access to care. Advocacy is essential for better policies and resources.
Orphan drugs have become a focal point in India's healthcare discussions, particularly following the National Policy for Rare Diseases (NPRD) established in 2021. This policy aimed to create...
