Charging for Investigational Drugs Under an Investigational New Drug Application
fda-drug · Food and Drug Administration · Rule · Published 2009-08-13 · Effective 2009-10-13 · 74 FR 40872
Document
Document number
E9-19004
Federal Register citation
74 FR 40872
CFR reference
21 CFR 312
Type
Rule
Action
Final rule.
Category
fda-drug
Sub-agency
Food and Drug Administration
Publication date
2009-08-13
Effective date
2009-10-13
HHS docket
Docket No. FDA-2006-N-0237
Abstract
The Food and Drug Administration (FDA) is amending its investigational new drug application (IND) regulation concerning charging patients for investigational new drugs. This final rule revises the charging regulation to clarify the circumstances in which charging for an investigational drug in a clinical trial is appropriate, to set forth criteria for charging for an investigational drug for the different types of expanded access for treatment use described in the agency's final rule on expanded access for treatment use of investigational drugs published elsewhere in this issue of the Federal Register, and to clarify what costs can be recovered for an investigational drug. This final rule will permit charging for a broader range of uses than was explicitly permitted previously.