| 紀錄類型: |
書目-語言資料,印刷品
: Monograph/item
|
| 杜威分類號: |
615.19 |
| 書名/作者: |
Quality control training manual : comprehensive training guide for API, finished pharmaceutical and biotechnologies laboratories // Syed Imtiaz Haider, Erfan Asif Syed. |
| 作者: |
Haider, Syed Imtiaz. |
| 其他作者: |
Asif, Erfan Syed. |
| 出版者: |
Boca Raton : : CRC Press,, 2011. |
| 面頁冊數: |
1 online resource (xxix, 456 p.) : : ill. |
| 標題: |
Medical laboratories - Standards. |
| 標題: |
Pharmaceutical technology - Standards. |
| 標題: |
Medical laboratories - Examinations, questions, etc. |
| 標題: |
Pharmaceutical technology - Examinations, questions, etc. |
| 標題: |
Laboratories - Examination Questions. - standards |
| 標題: |
Technology, Pharmaceutical - Handbooks. - standards |
| 標題: |
Biotechnology - Examination Questions. - standards |
| 標題: |
Drug Industry - Handbooks. - standards |
| 標題: |
Pharmaceutical Preparations - Handbooks. - standards |
| 標題: |
Quality Control - Handbooks. |
| ISBN: |
9781439850169 (electronic bk.) |
| ISBN: |
143985016X (electronic bk.) |
| 書目註: |
Includes bibliographical references and index. |
| 內容註: |
Qct-01. Analytical methods, techniques and quality measures for general pharmaceutical products -- qct-02. Analytical methods, techniques and quality measures for biological products -- qct-03. Laboratory training manual -- qct-04. Assessment of training -- qct-05. Training assessment with quiz and answers -- qct-06. Training log -- qct-07. Analytical method validation master plan -- qct-08. Analytical methods validation protocol -- qct-09. SOP for annual re-qualification of HPLC units -- qct-10. SOP for annual re-qualification of GC units -- qct-11. ABC pharmaceutical company -- qct-12. Regulations. |
| 摘要、提要註: |
"Written to help companies comply with GMP, GLP, and validation requirements imposed by the FDA and regulatory bodies worldwide, Quality Control Training Manual: Comprehensive Training Guide for API, Finished Pharmaceutical and Biotechnologies Laboratories presents cost-effective training courses that cover how to apply advances in the life sciences to produce commercially viable biotech products and services in terms of quality, safety, and efficacy. This book and its accompanying CD-ROM comprise detailed text, summaries, test papers, and answers to test papers, providing an administrative solution for management. Provides the FDA, Health Canada, WHO, and EMEA guidelines directly applicable to pharmaceutical laboratory-related issues. Offers generic formats and styles that can be customized to any organization and help management build quality into routine operations to comply with regulatory requirements. Contains ready-to-use training courses that supply a good source of training material for experienced and inexperienced practitioners in the biotechnology/biopharmaceutical industries. Includes a CD with downloadable training courses that can be adopted and directly customized to a particular organization. Supplies ready-to-use test papers that allow end users to record all raw data up to the issuance of the attached certificate. The biotechnology/bioscience industries are regulated worldwide to be in compliance with cGMP and GLP principles, with particular focus on safety issues. Each company must create a definite training matrix of its employees. The training procedures in this book enable end users to understand the principles and elements of manufacturing techniques and provide documentation language ranging from the generic to the specific. The training courses on the CD supply valuable tools for developing training matrices to achieve FDA, Health Canada, EMEA, MHRA UK, WHO, and GLP compliance"--Provided by publisher. |
| 電子資源: |
http://www.crcnetbase.com/isbn/978-1-4398-4994-1 |