Handbook of modern pharmaceutical analysis
tarafından
 
Ahuja, Satinder, 1933- editor.

Başlık
Handbook of modern pharmaceutical analysis

Yazar
Ahuja, Satinder, 1933- editor.

ISBN
9780123759818
 
9781282879027
 
9786612879029

Basım Bilgisi
2nd edition.

Yayın Bilgileri
Amsterdam ; Boston : Academic Press/Elsevier, 2011.

Fiziksel Tanımlama
1 online resource (xv, 582 pages, 4 unnumbered pages of plates) : illustrations (some color)

Seri
Separation science and technology ; v. 10
 
Separation science and technology (San Diego, Calif.) ; v. 10.

İçerik
Overview / (Satinder Ahuja) -- High Throughput Screening in Drug Discovery and Development / (Ken Apple) -- Solid-State Analysis / (Harry Brittain) -- Degradation Studies of Drug Candidates / (Karen Alsante) -- Analytical Considerations for Genotoxic and Other Impurities / (Scott Miller) -- Quality by Design / (James Drennen) -- Preformulation Studies -- Process Analytical Technology / (Christine Richardson) -- Solid Dosage-Form Analysis / (Joe Etse) -- Parenteral Dosage Form Analysis / (Greg Birrer) -- Analysis of Alternate Drug Delivery systems / (Ron Smith) -- Method Development for Chiral Compounds / (S. Ahuja) -- Method Development for Early Phase Drug Development / (Kevin Bynum) -- Method Development for Late Phase Drug Development / (Ilias Jimidar) -- Analysis of Biomolecules / (Ilias Jimidar) -- Setting Up Specifications / (Doug Raynie) -- Validation of Test Methods / (Jonathan Crowther) -- Stability Evaluations / (Jessica Cha) -- Transferring Analytical Methods / (Stephen Scypinski) -- Pharmaceutical Analysis Documentation / (H. Chokshi) -- Emerging Analytical Methodologies / (Jim Lander).

Özet
Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. *Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it. *Covers method development, validation, selection, testing, modeling, and simulation studies combined with advanced exploration of assays, impurity testing, biomolecules, and chiral separations. *Features detailed coverage of QA, ethics, and regulatory guidance and structures, as well as high-tech methodologies and technologies from "lab-on-a-chip" to LC-MS, LC-NMR, and LC-NMR-MS.

Konu Başlığı
Pharmaceutical chemistry -- Handbooks, manuals, etc.
 
Drugs -- Analysis -- Handbooks, manuals, etc.
 
Drug development -- Handbooks, manuals, etc.
 
Chemistry, Pharmaceutical -- methods. (DNLM)D002626Q000379
 
Pharmaceutical Preparations -- analysis. (DNLM)D004364Q000032
 
Technology, Pharmaceutical -- methods. (DNLM)D013678Q000379
 
MEDICAL -- Drug Guides.
 
MEDICAL -- Pharmacology.
 
MEDICAL -- Pharmacy.
 
MEDICAL -- Nursing -- Pharmacology.
 
Drug development. (OCoLC)fst00898670
 
Drugs -- Analysis. (OCoLC)fst00898769
 
Pharmaceutical chemistry. (OCoLC)fst01060115
 
Pharmazeutische Analyse (DE-588)4174139-0

Tür
Electronic books.
 
Handbooks and manuals. (OCoLC)fst01423877
 
Handbooks and manuals.

Added Author
Ahuja, Satinder, 1933-
 
Scypinski, Stephen,

Elektronik Erişim
ScienceDirect https://www.sciencedirect.com/science/book/9780123756800
 
ScienceDirect https://www.sciencedirect.com/science/bookseries/18771718/10


Yer NumarasıDemirbaş NumarasıShelf LocationShelf LocationHolding Information
RS404.5 .H36 2011 EB1183536-1001Elsevier E-Kitap KoleksiyonuElsevier E-Kitap Koleksiyonu