Wall g michael (30 Ergebnisse)

Soft cover. Zustand: Very Good. First Collected Edition, PBO thus.. **FEATURE AND NOVELETS (1) The Stalker of Biscayne Bay by Brett Halliday (2) Assassination - Middle East by Joseph Commings **STORIES (1) In The Key Of Murder by Hal Charles (2) Whistle by Mignon Glass (3) Dont Dare Reject This Manuscript by William Schoell (4) Animal Sounds by Don Wall (5) Delayed Verdict by R. C. Tuttle (6) Saturday Night Special by Terry Black>> Creasing to front cover. Size: 12mo - over 6¾" - 7¾" tall. Keller GGA Painted Cover. (illustrator). Book.…

Soft cover. Zustand: Very Good to Fine. First Collected Edition, PBO thus.. **FEATURE AND NOVELETS (1) The Stalker of Biscayne Bay by Brett Halliday (2) Assassination - Middle East by Joseph Commings **STORIES (1) In The Key Of Murder by Hal Charles (2) Whistle by Mignon Glass (3) Dont Dare Reject This Manuscript by William Schoell (4) Animal Sounds by Don Wall (5) Delayed Verdict by R. C. Tuttle (6) Saturday Night Special by Terry Black>> Slight spine slant; Indents to front cover; scuffing to backcover. Size: 12mo - over 6¾" - 7¾" tall. Keller GGA Painted Cover. (illustrator). Book.…

Soft cover. Zustand: Near Fine. First Collected Edition, PBO thus.. **FEATURE AND NOVELETS (1) The Stalker of Biscayne Bay by Brett Halliday (2) Assassination - Middle East by Joseph Commings **STORIES (1) In The Key Of Murder by Hal Charles (2) Whistle by Mignon Glass (3) Dont Dare Reject This Manuscript by William Schoell (4) Animal Sounds by Don Wall (5) Delayed Verdict by R. C. Tuttle (6) Saturday Night Special by Terry Black Size: 12mo - over 6¾" - 7¾" tall. Keller GGA Painted Cover. (illustrator). Book.…

Softcover. Zustand: Very Good. No Dust Jacket. First Edition. ISSN 0143-2974. Contents include: Editorial: search room closures; County record office closures; News from the Cambridge group for the history of population and social structure; Person mobility in three West Riding parishes 1777-1812; Distance to church and registration experience; Notes and queries: age at baptism in the London parish of St Olave Old Jewry; birth baptism intervals in some Flintshire parishes; Local research in progress. Crisp cream illustrated covers with previous owner's details in top corner, sound stapled binding, clean pages. No dust jacket, as published. Quantity Available: 1. Shipped Weight: under 1 kg. Pictures of this item not already displayed here available upon request. Inventory No: 42012060151. All our books are sent by tracked mail. …

Zustand: Brand New. New.SoftCover International edition. Different ISBN and Cover image but contents are same as US edition.Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

Hardcover. Zustand: Fine. Zustand des Schutzumschlags: Fine. 1st Edition. Title page. List of contributors: Patricia Redmond, Henry Louis Gates, Jr., Barbara E. Johnson, Donald B. Gibson, Deborah E. McDowell, Hortense J. Spillers, Michael Awkward, William L. Andrews, Sandra Pouchet Paquet, Genevieve Fabre, Richard Yarborough, Robert B. Stepto, Eleanor W. Traylor, Housron A. Baker, Jr., Mae G. Hewnderson, Kimberly W. Benston, Cheryl A. Wall, Stephen E. Henderson, Arnold Rampersad, Michel Fabre, Nellie Y. McKay, Robert G. O'Meally. Afterword by Houston AFine blue orange dust jacket with title and contributing . Title on dust jacket pine panel. authors. Baker, Jr. and Patricia Redmond. Index. 246pp. Blue cloth boards with bright silver title on spine.…

Hardcover. Zustand: Used: Very Good. 1st Edition. Very good.

Zustand: New.

Zustand: New.

Zustand: New. In English.

Zustand: New. In English.

Taschenbuch. Zustand: Neu. Pharmaceutical Suspensions | From Formulation Development to Manufacturing | Alok K. Kulshreshtha (u. a.) | Taschenbuch | xvi | Englisch | 2014 | Springer US | EAN 9781489984173 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. …

Zustand: New. pp. 344.

Hardcover. Zustand: Brand New. 1st edition. 327 pages. 9.25x6.25x1.00 inches. In Stock.

Hardcover. Zustand: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Paperback. Zustand: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Zustand: As New. Unread book in perfect condition.

Zustand: As New. Unread book in perfect condition.

Zustand: new. Questo è un articolo print on demand.

Zustand: new. Questo è un articolo print on demand.

Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Written by experienced experts in applicable field from academia/industry/regulatory agencies, volume will systematically discuss the development of stable pharmaceutical suspensionsALOK K. KULSHRESHTHA, Ph.D., Associate Direc. …

Gebunden. Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Written by experienced experts in applicable field from academia/industry/regulatory agencies, volume will systematically discuss the development of stable pharmaceutical suspensionsALOK K. KULSHRESHTHA, Ph.D., Associate Direc.…

Buch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The suspension dosage form has long been used for poorly soluble active ingre- ents for various therapeutic indications. Development of stable suspensions over the shelf life of the drug product continues to be a challenge on many fronts. A good understanding of the fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of a s- pension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, visco- ters, particle size analyzers, etc.) must be utilized to properly characterize the s- pension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require cli- cal trials to establish the safety and efficacy of the drug product. All of this devel- ment work should culminate into a regulatory filing in accordance with the regulatory guidelines. Pharmaceutical Suspensions, From Formulation Development to Manufacturing, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system - poorly soluble active pharmaceutical ingredients s- pended in a suitable vehicle. 344 pp. Englisch.…

Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The suspension dosage form has long been used for poorly soluble active ingre- ents for various therapeutic indications. Development of stable suspensions over the shelf life of the drug product continues to be a challenge on many fronts. A good understanding of the fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of a s- pension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, visco- ters, particle size analyzers, etc.) must be utilized to properly characterize the s- pension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require cli- cal trials to establish the safety and efficacy of the drug product. All of this devel- ment work should culminate into a regulatory filing in accordance with the regulatory guidelines. Pharmaceutical Suspensions, From Formulation Development to Manufacturing, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system - poorly soluble active pharmaceutical ingredients s- pended in a suitable vehicle. 344 pp. Englisch.…

Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The suspension dosage form has long been used for poorly soluble active ingre- ents for various therapeutic indications. Development of stable suspensions over the shelf life of the drug product continues to be a challenge on many fronts. A good understanding of the fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of a s- pension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, visco- ters, particle size analyzers, etc.) must be utilized to properly characterize the s- pension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require cli- cal trials to establish the safety and efficacy of the drug product. All of this devel- ment work should culminate into a regulatory filing in accordance with the regulatory guidelines. Pharmaceutical Suspensions, From Formulation Development to Manufacturing, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system - poorly soluble active pharmaceutical ingredients s- pended in a suitable vehicle.…

Buch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The suspension dosage form has long been used for poorly soluble active ingre- ents for various therapeutic indications. Development of stable suspensions over the shelf life of the drug product continues to be a challenge on many fronts. A good understanding of the fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of a s- pension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, visco- ters, particle size analyzers, etc.) must be utilized to properly characterize the s- pension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require cli- cal trials to establish the safety and efficacy of the drug product. All of this devel- ment work should culminate into a regulatory filing in accordance with the regulatory guidelines. Pharmaceutical Suspensions, From Formulation Development to Manufacturing, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system - poorly soluble active pharmaceutical ingredients s- pended in a suitable vehicle.…

Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The suspension dosage form has long been used for poorly soluble active ingre- ents for various therapeutic indications. Development of stable suspensions over the shelf life of the drug product continues to be a challenge on many fronts. A good understanding of the fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of a s- pension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, visco- ters, particle size analyzers, etc.) must be utilized to properly characterize the s- pension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require cli- cal trials to establish the safety and efficacy of the drug product. All of this devel- ment work should culminate into a regulatory filing in accordance with the regulatory guidelines. Pharmaceutical Suspensions, From Formulation Development to Manufacturing, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system ¿ poorly soluble active pharmaceutical ingredients s- pended in a suitable vehicle.Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 344 pp. Englisch.…

Buch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The suspension dosage form has long been used for poorly soluble active ingre- ents for various therapeutic indications. Development of stable suspensions over the shelf life of the drug product continues to be a challenge on many fronts. A good understanding of the fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of a s- pension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, visco- ters, particle size analyzers, etc.) must be utilized to properly characterize the s- pension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require cli- cal trials to establish the safety and efficacy of the drug product. All of this devel- ment work should culminate into a regulatory filing in accordance with the regulatory guidelines. Pharmaceutical Suspensions, From Formulation Development to Manufacturing, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system ¿ poorly soluble active pharmaceutical ingredients s- pended in a suitable vehicle.Springer-Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 344 pp. Englisch.…

Zustand: New. Print on Demand pp. 344.

Zustand: New. PRINT ON DEMAND pp. 344.