Regulatory Issues in Chromatographic Analysis in the Pharmaceutical Industry-Reference-Cited by-同舟云学术

Regulatory Issues in Chromatographic Analysis in the Pharmaceutical Industry

Published:2004-01 Issue:7-9 Volume:27 Page:1413-1442
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Dantus Mauricio M.¹,Wells Margaret L.¹

Affiliation:

1. a Merck and Company , RY818‐C221, P.O. Box 2000, Rahway , New Jersey , 07065 , USA

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/JLC-120030610

Reference95 articles.

1. 1996.Federal Register 21 CFR Parts 210 and 211 Current Good Manufacturing Practice: Amendment of Certain Requirements for Finished Pharmaceuticals; Proposed RuleVol. 61, 20104–20115. Food and Drug Administration. 87

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