Research Catalog

Title

Guidance for industry : gene therapy clinical trials, observing subjects for delayed adverse events.

Publication

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

Details

Additional Authors

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

Description

i, 23 pages : digital, PDF file

Alternative Title

Gene therapy clinical trials, observing subjects for delayed adverse events

Subject

• Gene therapy > United States
• Clinical trials > Government policy > United States

Note

• Title from PDF title page (viewed on May 12, 2009).
• "November 2006".

Bibliography (note)

• Includes bibliographical references (page 23).

System Details (note)

• Mode of access: Internet at the FDA CBER web site. Address as of 5/12/09: http://www.fda.gov/cber/gdlns/gtclin.pdf ; current access is available via PURL.

Call Number

GPO Internet HE 20.4802:G 28/3

OCLC

marcive320816600

Title

Guidance for industry : gene therapy clinical trials, observing subjects for delayed adverse events.

Publisher

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

Type of Content

text

Type of Medium

computer

Type of Carrier

online resource

System Details

Mode of access: Internet at the FDA CBER web site. Address as of 5/12/09: http://www.fda.gov/cber/gdlns/gtclin.pdf ; current access is available via PURL.

Bibliography

Includes bibliographical references (page 23).

Connect to:

https://purl.fdlp.gov/GPO/LPS112486

Added Author

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

Gpo Item No.

0499-T-02 (online)

Sudoc No.

HE 20.4802:G 28/3