Research Catalog

Title

Guidance for industry : compliance with 21 CFR part 1271.150(c)(1), manufacturing arrangements.

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, 3 pages : digital, PDF file

Alternative Title

Compliance with 21 CFR part 1271.150(c)(1), manufacturing arrangements

Subject

• Human cell culture > Government policy > United States
• Tissue engineering > Government policy > United States

Note

• Title from PDF title page (viewed on May 18, 2009).
• "September 2006".

Bibliography (note)

• Includes bibliographical references (page 3).

System Details (note)

• Mode of access: Internet at the FDA CBER web site. Address as of 5/18/09: http://www.fda.gov/cber/gdlns/cgtpmanuf.pdf ; current access is available via PURL.

Call Number

GPO Internet HE 20.4802:C 73/4

OCLC

marcive325057001

Title

Guidance for industry : compliance with 21 CFR part 1271.150(c)(1), manufacturing arrangements.

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 5/18/09: http://www.fda.gov/cber/gdlns/cgtpmanuf.pdf ; current access is available via PURL.

Bibliography

Includes bibliographical references (page 3).

Connect to:

https://purl.fdlp.gov/GPO/LPS112732

Added Author

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

Gpo Item No.

0499-T-02 (online)

Sudoc No.

HE 20.4802:C 73/4