Policies & Guidelines
Policies relating to rare diseases are significant in its ability to transform patient lives. By formulating and implementing pro-rare disease policies; patients will be able to access quality treatment and care, better access to drugs and clinical trials, multidisciplinary care and psychosocial support.
India is still in the nascent stage of a clearcut National Rare Disease Policy guidelines. Since health is a state subject, each state has come up with a set of policies to improve patient care and access to treatment.
It is also significant that rare diseases like the blood and bleeding disorders, muscular dystrophies and multiple sclerosis have been included in the Rights of People with Disabilities Act 2016. This will not only improve and strengthen healthcare practices but also provide legal support to children and adults in accessing education and other services in the country.
Downloadable policies and guidelines:
- National Policy for Treatment of Rare Diseases (Download PDF)
- National Guidelines on Hemoglobinopathies in India (Download PDF)
- Rights of People with Disabilities Act 2016 (Download PDF)
- Blood Guidelines India (Download PDF)
- Karnataka Day Care Centres Guidelines (Download PDF)
- Karnataka Antenatal Screening for Thalassemia Guidelines (Download PDF)