Quality control training manual : comprehensive training guide for API, finished pharmaceutical and biotechnologies laboratories / Syed Imtiaz Haider, Erfan Syed Asif.
Material type:![Text](/opac-tmpl/lib/famfamfam/BK.png)
- 9781439849941
- Biotechnology
- Biotechnology
- Drug Industry
- Drug Industry
- Laboratories
- Laboratories
- Medical laboratories
- Medical laboratories
- Pharmaceutical Preparations
- Pharmaceutical Preparations
- Pharmaceutical technology
- Pharmaceutical technology
- Quality Control
- Quality Control
- Technology, Pharmaceutical
- Technology, Pharmaceutical
- RS 192 .H124 2011
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Aklatang Emilio Aguinaldo-Information Resource Center Reference | RS 192 .H124 2011 (Browse shelf(Opens below)) | Not for loan | 3AEA2013001406 |
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RM 723.T45 .M315 2002 Thai bodywork / | RS 51.M537 1996 The Merck index : an encyclopedia of chemicals, drugs, and biologicals/. | RS 51 .P569 1993 Physicians' desk reference : PDR. | RS 192 .H124 2011 Quality control training manual : comprehensive training guide for API, finished pharmaceutical and biotechnologies laboratories / | RZ 401 .W153 2003 Healing massage : a simple approach / | RZ 401 .W153 2003 Healing massage : a simple approach / | RZ 440 .F413 2004 Natural remedies encyclopedia : [home remedies for over 730 diseases] / |
Includes bibliographical references and index.
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
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