[Federal Register Volume 59, Number 240 (Thursday, December 15, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: X94-21215]


[[Page Unknown]]

[Federal Register: December 15, 1994]


      
                                                   VOL. 59, NO. 240

                                        Thursday, December 15, 1994

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration
[Docket No. 85D-0505]

 

Guideline for Adverse Experience Reporting for Licensed 
Biological Products; Availability

Correction

    In notice document 94-26484 appearing on page 53994, in the issue 
of Thursday, October 27, 1994, make the following corrections:
    1.On page 53994, in the second column, under SUPPLEMENTARY 
INFORMATION:, in the first full paragraph, in the third line, ``with'' 
should read ``will''.
    2.On the same page, in the same column, in the second paragraph, in 
the first line, ``guidelines'' should read ``guideline''.

BILLING CODE 1505-01-D