Nicht aus der Schweiz? Besuchen Sie lehmanns.de
Handbook of Pharmaceutical Manufacturing Formulations - Sarfaraz K. Niazi

Handbook of Pharmaceutical Manufacturing Formulations

Volume Three, Liquid Products
Buch | Hardcover
400 Seiten
2009 | 2nd New edition
Informa Healthcare (Verlag)
978-1-4200-8123-7 (ISBN)
CHF 287,95 inkl. MwSt
zur Neuauflage
  • Titel erscheint in neuer Auflage
  • Artikel merken
Zu diesem Artikel existiert eine Nachauflage
Handbook of Pharmaceutical Manufacturing Formulations
While liquid drugs do not share the compression problems of solid dosage forms, the filling problems of powder dosage forms, or the consistency problems of semisolid dosage forms, they do have their own set of considerations in the formulation and manufacturing stages.


Highlights from Liquid Products, Volume Three include:




practical details involved in complying with the current good manufacturing practice requirements in liquid manufacturing
access to what an FDA auditor would be looking for during a liquid manufacturing audit
issues that may arise during a US FDA inspection
the protocols used for stability testing for new drugs and new dosage forms, drawn from the most current ICH guidelines

REGULATORY AND MANUFACTURING GUIDANCE
Manufacturing Practice Considerations in Liquid Formulations
Oral Solutions and Suspensions
The FDA Drug Product Surveillance Program
Changes to Approved NDAs and ANDAs
Formulation Considerations of Liquid Products
Container Closure Systems
Material for Containers
Stability Testing of New Drug Substances and Products
Stability Testing: Photostability Testing of New Drug Substances and Products
Stability Testing for New Dosage Forms
Bracketing and Matrixing Designs for Stability Testing of New Drug Substances and Products
Evaluation of Stability Data
Stability Data Package for Registration Applications in Climatic Zones III and IV
EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use
EDQM Certification
Impurities: Guideline for Residual Solvents
Electronic Records and Signatures (CFR 21 Part 11 Compliance)
GMP Audit Template, EU Guidelines
Bioequivalence Testing Protocols
Dissolution Testing of Liquid Dosage Forms
Approved Excipients in Liquid Forms

MANUFACTURING FORMULATIONS
Manufacturing Formulations

Erscheint lt. Verlag 21.9.2009
Zusatzinfo 3 Illustrations, black and white
Verlagsort New York
Sprache englisch
Maße 216 x 279 mm
Gewicht 1452 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
Medizin / Pharmazie Pflege
Medizin / Pharmazie Pharmazie
Technik
ISBN-10 1-4200-8123-3 / 1420081233
ISBN-13 978-1-4200-8123-7 / 9781420081237
Zustand Neuware
Informationen gemäß Produktsicherheitsverordnung (GPSR)
Haben Sie eine Frage zum Produkt?
Mehr entdecken
aus dem Bereich