ARCHIVES

FDA Simplifies Reporting Of Adverse Events

This article is from The Cancer Letter archive.

Vol. 19 No. 25 | June 18, 1993

Download PDF Visit The Full Archive

Related Articles

White House Order Poses Difficulties For NIH Peer Review

April 2, 1993

More Concept Approvals By DCPC Board

May 18, 1984

FDA Approves Gleevec In 73 Days, A Speed Record.

May 18, 2001

ACOS Planning Patient Care Melanoma Study

August 4, 1989

Breast Cancer Action Plan Committee Outrages By Plans for $14M In NCI Funds

August 1, 1997

NCI Makes Its Pitch To OMB For Its First Billion Dollar Budget; Research Areas Listed By Priority

October 14, 1977