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Biomedical Product Development: Bench to Bedside

Overview of attention for book
Cover of 'Biomedical Product Development: Bench to Bedside'

Table of Contents

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    Book Overview
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    Chapter 1 An Introduction to Biomedical Product Development
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    Chapter 2 Basic Essentials and Applications of Quality Management System (QMS) in Biomedical Sciences
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    Chapter 3 Principles of Good Laboratory Practice (GLP)
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    Chapter 4 Design of Experimental Studies in Biomedical Sciences
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    Chapter 5 Preclinical Studies for Development of Biomedical Products
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    Chapter 6 Principles of Good Manufacturing Practice
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    Chapter 7 The Importance of Cleanroom Facility in Manufacturing Biomedical Products
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    Chapter 8 Safety Concerns and Requirement of Cell-Based Products for Clinical Application
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    Chapter 9 Standards and Regulatory Frameworks (for Cell- and Tissue-Based Products)
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    Chapter 10 Principles of Good Clinical Practice
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    Chapter 11 Design, Performance, and Monitoring of Clinical Trials
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    Chapter 12 Good Clinical Practice: Guidelines and Requirements
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    Chapter 13 Ethical Considerations of Biomedical Product Development
Attention for Chapter 9: Standards and Regulatory Frameworks (for Cell- and Tissue-Based Products)
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