Skip to main content
Log in

The Patient Advocate Perspective on Preparing for FDA Advisory Committee Presentations

  • Published:
Drug information journal : DIJ / Drug Information Association Aims and scope Submit manuscript

Abstract

This article highlights the author’s experiences as a patient advocate serving on the Food and Drug Administration (FDA) Biological Response Modifiers Committee. It provides an overview of the National Organization for Rare Disorders and the scope of the orphan disease problem. The author explains the process of serving on an advisory committee, and highlights the important role of patient advocates in protecting the patient’s best interests.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Abbey S. Meyers.

Additional information

Presented at the DIA 35th Annual Meeting, June 27–July 1, 1999, Baltimore, Maryland.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Meyers, A.S. The Patient Advocate Perspective on Preparing for FDA Advisory Committee Presentations. Ther Innov Regul Sci 34, 969–973 (2000). https://doi.org/10.1177/009286150003400330

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1177/009286150003400330

Key Words

Navigation