National Organization for Rare Disorders
55 Kenosia Avenue
Danbury
Connecticut
06810
United States
Tel: 203-744-0100
Fax: 203-263-9938
Website: https://rarediseases.org/
63 articles with National Organization for Rare Disorders
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Horizon Pharma and the National Organization for Rare Disorders (NORD) launched a new campaign today that recognizes innovation in rare disease therapeutics since the passing of the Orphan Drug Act in 1983.
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NORD Launches RareInsights - New Initiative to Support Data-Driven Advocacy, and Presents "5 Myths About Orphan Drugs and the Orphan Drug Act"
5/30/2018
The National Organization for Rare Disorders (NORD) today launched RareInsights™.
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New Report Shows States Fall Short on Policies to Help Reduce Burden of Rare Diseases Affecting 1 in 10 Americans
3/20/2018
A majority of states are not measuring up on legislative solutions that reduce the burden of rare diseases affecting 30 million Americans, according to a new report released today by the National Organization for Rare Disorders Rare Action Network™ (NORD RAN).
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NORD to Collaborate with FDA on Pilot Patient Engagement Activity
2/28/2018
Listening Sessions to Enable Sharing Rare Disease Experiences with FDA Review Divisions
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Incyte Supports the Myeloproliferative Neoplasm Community in Honor of Rare Disease Day 2018
2/28/2018
“Beyond Blue,” a short documentary by an award-winning filmmaker, debuts to raise awareness of MPNs MPN Heroes® 2018 nominations now open for submission
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National Organization for Rare Disorders Launches Free CME Program To Educate Medical Professionals About Rare Diseases
5/9/2017
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Research Grants Available For Rare Diseases From National Organization for Rare Disorders
4/26/2017
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National Organization for Rare Disorders Release: Report Shows Majority Of States Fall Short On Policies To Help Reduce Burden Of Rare Diseases Affecting 30 Million Americans
12/13/2016
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Cydan Development Celebrates Rare Disease Day With Gift To Support The National Organization for Rare Disorders Natural History Project
2/29/2016
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Medunik Canada Is Pleased To Announce The Launch Of National Organization for Rare Disorders Founder, Abbey Meyers' Memoir "Orphan Drugs: A Global Crusade"
2/16/2016
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FDA Awards National Organization for Rare Disorders $250,000 Grant To Support The Development Of 20 Natural History Studies For Rare Disease Research
12/10/2015
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National Organization for Rare Disorders Publishes Guide To Promote Physician Awareness Of Rare Lung Disorder
10/28/2015
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National Organization for Rare Disorders Releases First-Ever State Progress Report For Rare Diseases
10/23/2015
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New Video From National Organization for Rare Disorders Promotes Awareness Of Rare Movement Disorder Neurogenic Orthostatic Hypotension
8/25/2015
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Keynote Speakers Announced For National Organization for Rare Disorders's Rare Diseases & Orphan Products Breakthrough Summit
8/20/2015
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National Organization for Rare Disorders And University of Maryland Partner On PCORI Award To Advance Rare Disease Research
7/17/2015
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Research Grants For Rare Disease Research Available From National Organization for Rare Disorders; Deadline To Submit Abstracts Or Letters Of Intent Is July 31
7/15/2015
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Soligenix Announces Collaboration With The National Organization for Rare Disorders And The Cutaneous Lymphoma Foundation In Advancing Its Phase 3 Study Of SGX301 For The Treatment Of Cutaneous T-Cell Lymphoma
6/23/2015
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New White Paper From BIO, National Organization for Rare Disorders, And Ernst & Young LLP Finds Orphan Drug Tax Credit Is Crucial To Rare Disease R&D
6/17/2015
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Neurotrope Joins National Organization for Rare Disorders (NORD) Corporate Council
4/24/2015