Cargando…

Analytical Scientists in Pharmaceutical Product Development Task Management and Practical Knowledge.

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Xiao, Kangping
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Newark : John Wiley & Sons, Incorporated, 2020.
Temas:
Acceso en línea:Texto completo

MARC

LEADER 00000cam a2200000Mu 4500
001 EBOOKCENTRAL_on1202481099
003 OCoLC
005 20240329122006.0
006 m o d
007 cr cnu---unuuu
008 201031s2020 xx o ||| 0 eng d
040 |a EBLCP  |b eng  |c EBLCP  |d EBLCP  |d N$T  |d OCLCO  |d OCLCF  |d OCL  |d OCLCO  |d OCLCQ  |d OCLCO  |d OCLCL 
020 |a 1119547857 
020 |a 9781119547853  |q (electronic bk.) 
029 1 |a AU@  |b 000072471931 
035 |a (OCoLC)1202481099 
050 4 |a RM301.25 
082 0 4 |a 615.19 
049 |a UAMI 
100 1 |a Xiao, Kangping. 
245 1 0 |a Analytical Scientists in Pharmaceutical Product Development  |h [electronic resource] :  |b Task Management and Practical Knowledge. 
260 |a Newark :  |b John Wiley & Sons, Incorporated,  |c 2020. 
300 |a 1 online resource (275 p.) 
500 |a Description based upon print version of record. 
505 0 |a 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 
505 8 |a 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 
505 8 |a 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 
505 8 |a 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 
505 8 |a 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 
590 |a ProQuest Ebook Central  |b Ebook Central Academic Complete 
650 0 |a Drug development. 
650 0 |a Analytical chemistry. 
650 6 |a Médicaments  |x Développement. 
650 6 |a Chimie analytique. 
650 7 |a chemical analysis.  |2 aat 
650 7 |a Analytical chemistry  |2 fast 
650 7 |a Drug development  |2 fast 
758 |i has work:  |a Analytical scientists in pharmaceutical product development (Text)  |1 https://id.oclc.org/worldcat/entity/E39PCFv4hj6P7JfxXtXPv8V7VC  |4 https://id.oclc.org/worldcat/ontology/hasWork 
776 0 8 |i Print version:  |a Xiao, Kangping  |t Analytical Scientists in Pharmaceutical Product Development : Task Management and Practical Knowledge  |d Newark : John Wiley & Sons, Incorporated,c2020  |z 9781119547822 
856 4 0 |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=6369776  |z Texto completo 
938 |a ProQuest Ebook Central  |b EBLB  |n EBL6369776 
938 |a EBSCOhost  |b EBSC  |n 2646650 
994 |a 92  |b IZTAP