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Book Cover
E-book
Author Xiao, Kangping

Title Analytical Scientists in Pharmaceutical Product Development Task Management and Practical Knowledge
Published Newark : John Wiley & Sons, Incorporated, 2020

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Description 1 online resource (275 p.)
Contents Cover -- Title Page -- Copyright Page -- Contents -- Preface -- Chapter 1 Pharmaceutical Development at a Glance -- 1.1 Prescription Medicinal Product Development -- 1.1.1 Active Pharmaceutical Ingredient (API) Development -- 1.1.2 Preclinical Research -- 1.1.3 Clinical Research - Phase 1, Safety and Dosage -- 1.1.4 Clinical Research - Phase 2, Efficacy and Side Effects -- 1.1.5 Clinical Research - Phase 3, Efficacy and Monitoring of Adverse Reactions -- 1.1.6 Clinical Research - Phase 4, Post-Market Safety Monitoring -- 1.1.7 FDA Approval of a Prescription Medicine
1.2 Over-the-Counter (OTC) Medicinal Product Development -- 1.2.1 FDA Monograph System -- 1.2.2 New Drug Application Process for an OTC Medicinal Product -- 1.2.3 Clinical Trials in OTC Product Development -- 1.2.4 Prescription to OTC Switch -- References -- Chapter 2 Analytics in Fast-Paced Product Development -- 2.1 Overall Development Process for New Products -- 2.2 Regulatory Strategy and Analytical Development -- 2.2.1 NDA and ANDA Filing -- 2.2.2 Module 3 (CMC) of Common Technical Document -- 2.2.3 Supplements and Other Changes to an Approved NDA or ANDA
2.2.3.1 Major Changes -- Prior Approval Supplement -- 2.2.3.2 Moderate Changes -- CBE-30 -- 2.2.3.3 Moderate Changes -- CBE -- 2.2.3.4 Minor Changes -- Annual Report -- 2.2.4 Analytical Development with FDA Guidelines in Mind -- 2.3 ICH Guidelines and Analytical Development -- 2.4 Pharmacopoeia Monographs and Analytical Development -- 2.5 Formulation Development and Analytical Development -- 2.5.1 Method Development Based on an Ideal, Comprehensive Quality by Design -- 2.5.2 Fit-for-Purpose, Teamwork, Knowledge Sharing, and Platform Approach
2.6 Methods for Scale-Up and Manufacturing QC Laboratories -- 2.7 Process Analytical Technology -- 2.8 Quality Assurance, Compliance, and Analytical Development -- References -- Chapter 3 Effective, Efficient, and Innovative Analytical Development -- 3.1 Task Management by Fishbone Diagrams and Time-Bars -- 3.2 Project Management - Waterfall Versus Agile -- 3.3 Resource and Cost Estimations -- 3.4 Desired Skill Sets -- 3.5 Analytical Scientists and Innovation -- 3.5.1 Think Outside the Box -- 3.5.2 Think Inside the Box -- 3.5.3 Be Analytically Creative -- References
Chapter 4 Analytical Chemistry and Separation Science at Molecular Level -- 4.1 Ions and Ionic Strength -- 4.2 Protonation and Deprotonation -- 4.3 Hydrolysis of Salts -- 4.4 Charge-Dipole and Dipole-Dipole Interaction -- 4.5 Hydrogen Bonding -- 4.6 Electron Donor-Acceptor Interaction -- 4.7 Hydration and Solvation Energy -- 4.8 Hydrophobic Interactions -- 4.9 Events Happening on the Column Surface -- 4.10 Example Thought Processes of Chromatographic Method Development -- 4.10.1 General Considerations -- 4.10.2 Case Study - Method Development for Assay of Benzalkonium Chloride
Notes Description based upon print version of record
Subject Drug development.
Analytical chemistry.
chemical analysis.
Analytical chemistry
Drug development
Form Electronic book
ISBN 1119547857
9781119547853