Research Catalog

Details

Additional authors

1. Center for Drug Evaluation and Research (U.S.)
2. Center for Biologics Evaluation and Research (U.S.)
3. International Conference on Harmonisation.

Description

1. iv, 52 p. : digital, PDF file.

Alternative title

1. Q7A good manufacturing practice guidance for active pharmaceutical ingredients
2. Good manufacturing practice guidance for active pharmaceutical ingredients

Subject

1. Drug factories > Quality control
2. Pharmaceutical chemistry
3. Drugs > Quality control

Call number

1. GPO Internet HE 20.4702:M 31

Note

1. Title from PDF title page (viewed on June 17, 2009).
2. "ICH".
3. "August 2001".

System details (note)

1. Mode of access: Internet at the FDA web site. Address as of 6/17/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM129098.pdf ; current access is available via PURL.

Title

1. Guidance for industry [electronic resource] : Q7A good manufacturing practice guidance for active pharmaceutical ingredients.

Imprint

1. 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, [2001]

System details

1. Mode of access: Internet at the FDA web site. Address as of 6/17/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM129098.pdf ; current access is available via PURL.

Connect to:

1. http://purl.access.gpo.gov/GPO/LPS113849

Added author

1. Center for Drug Evaluation and Research (U.S.)
2. Center for Biologics Evaluation and Research (U.S.)
3. International Conference on Harmonisation.

Gpo item no.

1. 0499-T (online)

Sudoc no.

1. HE 20.4702:M 31

Research call number

1. GPO Internet HE 20.4702:M 31