Guidance for industry : patient-reported outcome measures, use in medical product development to support labeling claims.

Format:

Book

Government document

Contributor:

Center for Drug Evaluation and Research (U.S.)

Center for Biologics Evaluation and Research (U.S.)

Center for Devices and Radiological Health (U.S.)

Language:

English

Subjects (All):

Outcome assessment (Medical care)--United States.

Outcome assessment (Medical care).

Medical instruments and apparatus--Labeling--Government policy--United States.

Medical instruments and apparatus.

Drugs--Labeling--Government policy--United States.

Drugs.

United States.

Physical Description:

1 online resource (ii, 32 pages)

Other Title:

Patient-reported outcome measures, use in medical product development to support labeling claims

Place of Publication:

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research : Center for Devices and Radiological Health, [2006]

Notes:

Title from PDF title page (viewed on June 3, 2009).

"Draft guidance."

"Clinical/medical."

"February 2006."

OCLC:

369319736