Author:
Akl Magda A.,Ahmed Mona A.,Ramadan Ahmed
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference23 articles.
1. Guide to Inspections Validation of Cleaning Processes, U.S. Food and Drug Administration, (FDA), Office of Regulatory Affairs, Washington, DC, 1993, pp. 1–6, http://www.fda.gov//ora/inspect_ref/igs/valid.html (accessed 20.04.2009).
2. Development and validation of a liquid chromatographic method for the determination of the amlodipine residues on manufacturing equipment surfaces;Klinkenberg;J. Pharm. Biomed. Anal.,2003
3. Quantitative determination and sampling of azathioprine residues for cleaning validation in production area;Fazio;J. Pharm. Biomed. Anal.,2007
4. Cleaning level acceptance criteria and a high pressure liquid chromatography procedure for the assay of Meclizine Hydrochloride residue in swabs collected from pharmaceutical manufacturing equipment surfaces;Mirza;J. Pharm. Biomed. Anal.,1999
5. The Merck Index,2001
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