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IORD Advocacy: Customs Duty Waived on Import of Rare Disease Drugs & Special Food

    Home IORD in News IORD Advocacy: Customs Duty Waived on Import of Rare Disease Drugs & Special Food
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    Customs Duty Waived on Import of Rare Disease Drugs & Special Food

    IORD Advocacy: Customs Duty Waived on Import of Rare Disease Drugs & Special Food

    By IORD | IORD in News, IORD Updates, News, Rare Disease News | 0 comment | 1 April, 2023 | 0

    Thanks to the concerted efforts of national advocacy Indian Organization for Rare Diseases (IORD) towards the needs of rare disease patients and the community at large, the union finance ministry has now waived off basic customs duty on drugs and food items prescribed for special medical purposes that are imported for the treatment of rare diseases.

    Normally, drugs attract a basic customs duty of 10%, while some life-saving drugs and vaccines attract a concessional rate of 5% or are exempted entirely. 

    The Central Board of Indirect Taxes & Customs, Finance Ministry through its Notification No. 17/2023-Customs, has now provided relief to patients suffering from a range of rare diseases to import drugs and “special medical purpose” food listed under the National Policy for Rare Diseases, 2021. These formulations are intended to provide nutritional support to people suffering from a specific disease, disorder, or medical condition as part of their dietary management. Here is the copy of the Gazette Publication released on 29 March, 2023.

    Besides the anti-cancer drug Pembrolizumab (Keytruda), the Rare Diseases for which patients are now exempted from customs duties for importing drugs and “special medical purpose” food are mentioned in List No 38 of the Notification No. 17/2023-Customs

    They include the following:

    1. Lysosomal Storage Disorders (LSDs)

    2. Adrenoleukodystrophy

    3. Severe Combined Immunodeficiency (SCID)

    4. Chronic Granulomatous disease

    5.Wiskot Aldrich Syndrome

    6. Osteopetrosis

    7. Fanconi Anemia

    8. Laron’s Syndrome

    9. Tyrosinemia

    10. Glycogen storage disorders (GSD) I, III and IV due to 

    poor metabolic control, multiple liver adenomas, or high 

    risk for Hepatocellular carcinoma, or condition of substantial cirrhosis or liver dysfunction, or progressive liver failure

    11. Maple Syrup Urine Disease (MSUD)

    12. Urea cycle disorders

    13. Organic acidemias

    14. Autosomal recessive Polycystic Kidney Disease  

    15. Autosomal dominant Polycystic Kidney Disease 

    16.Phenylketonuria (PKU) 

    17. Non-PKU hyperphenylalaninemia conditions 

    18. Homocystinuria

    19. Urea Cycle Enzyme defects

    20.Glutaric Aciduria type 1 and 2

    21. Methyl Malonic Acidemia

    22.Propionic Acidemia

    23.Isovaleric Acidemia

    24. Leucine-sensitive hypoglycemia

    25. Galactosemia

    26.Glucose galactose malabsorbtion 

    27. Severe Food protein allergy

    28. GH deficiency

    29. Prader-Willi Syndrome

    30. Turner syndrome

    31. Noonan syndrome

    32. Acidemias, mitochondrial disorders

    33. Acute Intermittent Porphyria

    34. Wilson’s Disease 

    35. Congenital Adrenal Hyperplasia

    36. Neonatal onset Multisysteminflammatory Disease (NoMID)

    37. Gaucher Disease Type I and III

    38. Hurler Syndrome [Mucopolysaccharisosis (MPS) Type I]

    39. Hunter syndrome (MPS II)

    40. Pompe Disease

    41. Fabry Disease

    42. MPS IVA

    43. MPS VI

    44. Cystic Fibrosis

    45. Duchenne Muscular Dystrophy

    46. Spinal Muscular Atrophy

    47. Wolman Disease

    48. Hypophosphatasia

    49.Neuronal ceroid lipofuschinosis

    50. Hypophosphatemic Rickets

    51. Atypical Hemolytic Uremic Syndrome

    It may be recalled that in the past, import exceptions were available for drugs meant for use for treatment of Spinal Muscular Atrophy or Duchenne Muscular Dystrophy.

    How to Apply:

    To be eligible for this exemption, the individual importer must provide a certificate issued by the Director of Health Services at the Central or State level, or by the District Medical Officer/Civil Surgeon of their district. The proforma of the form to be used is mentioned in page 4 & 5 of the Customs Notification issued by the centre.

    Role of IORD:

    The Indian Organization for Rare Diseases (IORD) has been consistently advocating for mainstreaming “Rare Diseases” and “Orphan Drugs” into the government’s policies and schemes to benefit the community for a long time by making regular representations to the various stakeholders in the government.

    In a sample survey conducted by IORD in 2019, it found that 27% of people with a college degree, who live in urban areas with access to the internet including NRIs never heard these terms. Things have changed at least in India, in 2014 after President Abdul Kalam spoke about the awareness of rare diseases.

    Two years ago, IORD attended an important stakeholders’ meeting convened by the Union Ministry of Health and Family Welfare, Department of Health & Family Welfare (Drugs Regulation Section) at Nirman Bhawan, New Delhi in October 2020.

    The issue in question was the finalization of the draft rules G.S.R. 354(E), dated 05.06.2020 to amend the New Drugs and Clinical Trials Rules, 2019 to incorporate the provisions for compassionate use of new drugs in India that was represented by Prof Ramaiah Muthyala, IORD CEO & President. 

    Autoimmune diseases, Genetic Disorders, Inherited diseases, Lysosomal storage diseases, Metabolic disorders, Neurological disorders, Orphan diseases, Rare blood disorders, Rare cancers, rare disease awareness, Rare Disease Policy in India, Rare Diseases, Rare endocrine diseases, Rare eye diseases, Rare kidney diseases, Rare liver diseases, Undiagnosed diseases

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