The National Organization for Rare Disorders (NORD)


Database Subscriptions

Many libraries, schools, universities, and hospitals subscribe to NORD’s Rare Disease Database for unlimited access to reports on more than 1,150 diseases.

Index of Rare Diseases

This is the list of diseases currently covered in the Rare Disease Database.

Rare Disease Database

Search this database for reports on more than 1,150 diseases.

View sample report

Index of Organizations

This is the list of organizations in NORD’s Organizational Database.

Organizational Database

Read about more than 2,000 patient organizations and other sources of help.

NORD's
Washington Office

NORD's Washington OfficeRead about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC.

 

NORD Corporate Council Meeting Presentations

May 21, 2007 - Capital Hilton Hotel, Washington DC

Discussion: Follow-on Biologics and A Washington DC Update
Follow-on Biologics: A Patient Advocate's View

Shawn O'Neal, Associate
Vice President, Federal Government Relations,
National Multiple Sclerosis Society

Follow-on Biologics: Coalition View
(no presentation available)
William B. Schultz
Zuckerman Spaeder LLP

Follow-on Biologics: An Industry View
Audrey Phillips, PhD.
Executive Director,
BioPharmaceutical Public Policy Planning, Johnson & Johnson

Bio-Similars: A European Approach to Follow-on Biologics and Recent Drug Regulatory Development in EU
Yann Le Cam
Chief Executive Officer
European Organisation for Rare Diseases (EURORDIS)

To Be or Not to Be, Follow-on Biologics
Diane Dorman
Vice President Public Policy NORD

FDA Office of Orphan Product Development: An Update
Debra Y. Lewis OD
Acting Director
Office of Orphan Product Development, FDA

NIH Office of Rare Diseases: An Update
Stephen Groft, PharmD. Director,
Office of Rare Diseases, NIH

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Since 1983, working toward the prevention, treatment, and cure of rare “orphan” diseases.

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Last modified Thursday, November 05, 2009