The Resource Handbook of pharmaceutical manufacturing formulations, Volume 4, Semisolid products, Sarfaraz K. Niazi

Handbook of pharmaceutical manufacturing formulations, Volume 4, Semisolid products, Sarfaraz K. Niazi

Label
Handbook of pharmaceutical manufacturing formulations, Volume 4, Semisolid products
Title
Handbook of pharmaceutical manufacturing formulations
Title number
Volume 4
Title part
Semisolid products
Statement of responsibility
Sarfaraz K. Niazi
Title variation
Semisolid products
Creator
Subject
Genre
Language
eng
Summary
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 formulationsvaluable information on the difficult area of compliancechanges to appr
Cataloging source
N$T
Dewey number
615/.19
Illustrations
illustrations
Index
index present
LC call number
RS200
LC item number
.N53 2009eb vol. 4
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
  • handbooks
Label
Handbook of pharmaceutical manufacturing formulations, Volume 4, Semisolid 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
Part I -- Regulatory and Manufacturing Guidance -- 1 -- Waiver of In Vivo Bioequivalence Study -- 2 -- Quality Risk Management -- 3 -- Pharmaceutical Quality System -- 4 -- Pharmaceutical Development -- 5 -- Pharmaceutical Development in CTD -- 6 -- Scale-Up and Postapproval Changes for Nonsterile Semisolid Dosage Forms:Manufacturing Equipment -- 7 -- GOOD Manufacturing Practice Guide for Active Pharmaceutical Ingredients -- 8 -- Validation of Analytical Procedures -- 9 -- Validation of Analytical Procedures: Methodology -- 10 -- Bioequivalence Testing of Topical Drugs -- 11 -- Good Manufacturing Requirements for Active Pharmaceutical Ingredients -- 12 -- FDA Active Pharmaceutical Ingredient Manufacturing Facility Inspection -- 13 -- Specifications: Test Procedures and Acceptance Criteria for New DrugSubstances and New Drug Products -- 14 -- Skin Irritation and Sensitization Testing of Generic Transdermal Drug Products -- 15 -- Impurities in New Drug Substances -- 16 -Impurities in New Drug Products -- 17 -- Formulation Factors in Semisolid Dosage Forms -- 18 -- GMP Audit Template, EU Guidelines -- 19 -- Dissolution Testing of Semisolid Dosage Forms -- 20 -- Approved Excipients in Semisolid Dosage Forms -- Part II -- Manufacturing Formulations -- Regulatory and Manufacturing Guidance -- Index -- Back Cover
Control code
ocn502428165
Dimensions
unknown
Edition
2nd ed
Extent
1 online resource (xxi, 345 pages)
File format
unknown
Form of item
online
Isbn
9781420081275
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
.b24475105
Reformatting quality
unknown
Sound
unknown sound
Specific material designation
remote
System control number
  • (OCoLC)502428165
  • pebco1420081276

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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