Handbook of Pharmaceutical Manufacturing Formulations - Sarfaraz K. Niazi

Handbook of Pharmaceutical Manufacturing Formulations

Semisolid Products
Buch | Hardcover
376 Seiten
2009 | 2nd New edition
Informa Healthcare (Verlag)
978-1-4200-8126-8 (ISBN)
205,75 inkl. MwSt
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Handbook of Pharmaceutical Manufacturing Formulations
The fourth volume in the series covers the techniques and technologies involved in the preparation of semisolid products such as ointments, creams, gels, suppositories, and special topical dosage forms. Drug manufacturers need a thorough understanding of the specific requirements that regulatory agencies impose on the formulation and efficacy determination of drugs contained in these formulations.


Highlights from Semisolid Products, Volume Four include:




coverage of over 350 formulations
valuable information on the difficult area of compliance
changes to approved new drug applications and abbreviated new drug applications
the evolving guidelines of ICH and when to conduct a regulatory review

REGULATORY ANDMANUFACTURING GUIDANCE
Waiver of In Vivo Bioequivalence Study
Quality Risk Management
Pharmaceutical Quality System
Pharmaceutical Development
Pharmaceutical Development in CTD
Scale-Up and Postapproval Changes for Nonsterile Semisolid Dosage Forms: Manufacturing Equipment
GOOD Manufacturing Practice Guide for Active Pharmaceutical Ingredients
Validation of Analytical Procedures
Validation of Analytical Procedures: Methodology
Bioequivalence Testing of Topical Drugs
Good Manufacturing Requirements for Active Pharmaceutical Ingredients
FDA Active Pharmaceutical Ingredient Manufacturing Facility Inspection
Specifications: Test Procedures and Acceptance Criteria for New Drug Substances and New Drug Products: Chemical Substances
Skin Irritation and Sensitization Testing of Generic Transdermal Drug Products
Impurities in New Drug Substances
Impurities in New Drug Products
Formulation Factors in Semisolid Dosage Forms
GMP Audit Template, EU Guidelines
Dissolution Testing of Semisolid Dosage Forms
Approved Excipients in Semisolid Dosage Forms

MANUFACTURING FORMULATIONS
Regulatory and Manufacturing Guidance

Erscheint lt. Verlag 21.9.2009
Zusatzinfo 3 Illustrations, black and white
Verlagsort New York
Sprache englisch
Maße 216 x 279 mm
Gewicht 1338 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
Medizin / Pharmazie Pflege
Medizin / Pharmazie Pharmazie
Technik
ISBN-10 1-4200-8126-8 / 1420081268
ISBN-13 978-1-4200-8126-8 / 9781420081268
Zustand Neuware
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