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Date: 2018-12-18 Category: Extra Ordinary State: Union Government Country: India

Whereas the National Policy for Treatment of Rare Diseases 2017 is in force issued in June 2017

Issued by Ministry of Health and Family Welfare · Department of Health and Family Welfare

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Executive Summary & Key Takeaways

This notification, issued by the Ministry of Health and Family Welfare, Department of Health and Family Welfare on December 18, 2018, announces that the National Policy for Treatment of Rare Diseases, 2017, which was issued in June 2017, is being placed in abeyance. The Central Government has decided to review the policy based on new information and updates received, aiming for further improvement and effective implementation. The policy will remain in abeyance until a revised policy is issued or until further orders are given by the Central Government, whichever occurs first. The notification number is F.No. Z21026522018RD. The issuing authority is Manohar Agnani, Jt. Secy.

Key Entities Referenced

National Policy for Treatment of Rare Diseases, 2017: A policy issued in June 2017 by the Ministry of Health and Family Welfare, Department of Health and Family Welfare, that is currently in force but will be kept in abeyance until a revised policy or further orders are issued. Ministry of Health and Family Welfare: The Indian government ministry responsible for health policy in India, specifically the Department of Health and Family Welfare. Department of Health and Family Welfare: A department within the Ministry of Health and Family Welfare. Central Government: The government of India, which has decided to review and revise the National Policy for Treatment of Rare Diseases, 2017. New Delhi: The location where the notification regarding the National Policy for Treatment of Rare Diseases was issued, New Delhi, Delhi. MANOHAR AGNANI: Jt. Secy. (Joint Secretary) who is responsible for the notification.
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