Processing of peripheral blood progenitor cell components in improved clean areas does not reduce the rate of microbial contamination-Reference-Cited by-同舟云学术

Processing of peripheral blood progenitor cell components in improved clean areas does not reduce the rate of microbial contamination

Published:2002-01 Issue:1 Volume:42 Page:10-17
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Cassens Uwe,Ahlke Christoph,Garritsen Henk,Krakowitzky Petra,Wullenweber Jorg,Fischer Rudolf-Josef,Peters Georg,Sibrowski Walter

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1537-2995.2002.00013.x/fullpdf

Reference34 articles.

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2. 2. Transfusion Act of the Federal Republic of Germany. Federal Law Gazette 1. July 1998;I S.1752.

3. 3. Business Code for Pharmaceutical Enterprises. Federal Law Gazette 9. August 1994;I S.2071.

4. 4. Good Manufacturing Practices for Pharmaceutical Products of the World Health Organization. Thirty-second Report. Geneva: World Health Organization, 1992.

5. 5. Manufacture of Sterile Medicinal Products. Working Party on "Control of Medicines and Inspections": Revision of the Annex 1 to the EU Guide to Good Manufacturing Practice, Brussels, September 9, 1996.

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