The Resource Handbook of pharmaceutical manufacturing formulations, Volume 3, Liquid products, Sarfaraz K. Niazi

Handbook of pharmaceutical manufacturing formulations, Volume 3, Liquid products, Sarfaraz K. Niazi

Label
Handbook of pharmaceutical manufacturing formulations, Volume 3, Liquid products
Title
Handbook of pharmaceutical manufacturing formulations
Title number
Volume 3
Title part
Liquid products
Statement of responsibility
Sarfaraz K. Niazi
Title variation
Liquid products
Creator
Subject
Genre
Language
eng
Summary
With thoroughly revised and expanded content, this Second Edition six-volume set compiles volumes from FDA New Drug Applications, patent applications, and other sources of generic and proprietary formulations to cover the broad spectrum of issues concerning drug manufacturing
Cataloging source
N$T
Dewey number
615/.19
Illustrations
illustrations
Index
index present
LC call number
RS200
LC item number
.N53 2009eb vol. 3
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
  • handbooks
Label
Handbook of pharmaceutical manufacturing formulations, Volume 3, Liquid products, Sarfaraz K. Niazi
Publication
Antecedent source
unknown
Bibliography note
Includes bibliographical references and index
http://library.link/vocab/branchCode
  • net
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
  • Front Cover -- Volume 3; Preface to the Series-Second Edition; Preface to the Series-First Edition; About the Author; Contents; Part I -- Regulatory and Manufacturing Guidance; 1 -- Manufacturing Practice Considerations in Liquid Formulations; 2 -- Oral Solutions and Suspensions; 3 -- The FDA Drug Product Surveillance Program; 4 -- Changes to Approved NDAs and ANDAs; 5 -- Formulation Considerations of Liquid Products; 6 -- Container Closure Systems; 7 -- Material for Containers; 8 -- Stability Testing of New Drug Substances and Products
  • 18 -- GMP Audit Template, EU Guidelines19 -- Bioequivalence Testing Protocols; 20 -- Dissolution Testing of Liquid Dosage Forms; 21 -- Approved Excipients in Liquid Forms; Part II -- Manufacturing Formulations; Index; Back Cover -- Volume 3
  • 9 -- Stability Testing: Photostability Testing of New Drug Substances and Products10 -- Stability Testing for New Dosage Forms; 11 -- Bracketing and Matrixing Designs for Stability Testingof New Drug Substances and Products; 12 -- Evaluation of Stability Data; 13 -- Stability Data Package for Registration Applications in Climatic Zones III and IV; 14 -- EU Guidelines to Good Manufacturing Practice MedicinalProducts for Human and Veterinary Use; 15 -- EDQM Certification; 16 -- Impurities: Guideline for Residual Solvents; 17 -- Electronic Records and Signatures (CFR 21 Part 11 Compliance)
Control code
ocn502436317
Dimensions
unknown
Edition
2nd ed
Extent
1 online resource (xx, 377 pages)
File format
unknown
Form of item
online
Isbn
9781420081244
Level of compression
unknown
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other physical details
illustrations
Quality assurance targets
not applicable
http://library.link/vocab/recordID
.b24475099
Reformatting quality
unknown
Sound
unknown sound
Specific material designation
remote
System control number
  • (OCoLC)502436317
  • pebco1420081241

Library Locations

    • Deakin University Library - Geelong Waurn Ponds CampusBorrow it
      75 Pigdons Road, Waurn Ponds, Victoria, 3216, AU
      -38.195656 144.304955
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