Application of Project Management Principles to the Management of Pharmaceutical R&D Projects
Language: English
Published by Springer, 2020
Series: Book 13 of 13 - SpringerBriefs in Pharmaceutical Science & Drug Development
- Softcover
- New
Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
AbeBooks seller since August 14, 2006
Condition: New
£ 70.79
Quantity: 1 available
Add to basketItem description from seller
Druck auf Anfrage Neuware - Printed after ordering - Dr. Catalano has for the last ten years been doing consulting for the Pharmaceutical Industry. During his consulting he discovered that smallbusinesses such as, generic, startups, and virtual companies do not have the budget or the resources to apply the computer software utilized in project management and therefore do not apply project management principles in their business model. This reduces their effectiveness and increases their operating cost. Application of Project Management Principles to the Management of Pharmaceutical R&D Projects is presented as a paper-based system for completing all thecritical activities needed apply the project management system. This will allow these small businessto take advantage of the projectmanagement principles and gain all the advantages of the system. This book will be beneficial for beginners to understand the concepts of projectmanagement and for small pharmaceutical companies to apply the principlesof project management to their business model.…
Seller Inventory # 9783030575267
- Title
- Application of Project Management Principles to the Management of Pharmaceutical R&D Projects
- Author
- Thomas Catalano
- Publisher
- Springer
- Publication year
- 2020
- Condition
- Neu
- Binding
- Taschenbuch
- Language
- English
- ISBN 10
- 3030575268
- ISBN 13
- 9783030575267
- Item weight
- 149 grams
- Dimensions
- 235x155x6 mm
- Series
- Book 13 of 13: SpringerBriefs in Pharmaceutical Science & Drug Development
"Synopsis" may belong to another edition of this title.
About the Author
Dr. Catalano has over 37 years of experience in the pharmaceutical industry including positions such as Research Scientist, Group Leader Section Head, Associate Director ,Director ,Senior Director, and Consultant. He has managed the analytical support of Drug Substance and Drug Products, Pharmaceutical Development, Process Chemistry, Stability ,Assessment and Quality Assurance ( GMP, GLP, GCP ). His experience includes classical chemical and instrumental analyses, including MS hyphenated techniques such as GC/LC/MS, Solid State testing methodology and a thorough knowledge of cGMP’s, GLP’s, ICH guidance’s, USP, NF, and other global compendia/guidance’s. His leadership of several Global Pharmaceutical Sciences Teams for development projects involved directing the preparation of CMC documentation such as, IND, DMF, NDA, CTX, INDS, etc. for inclusion into regulatory documents, significant contributions to the registration of several currently marketed products e.g.Celebrex, Bextra, Dynastat, Inspra , Cytotec, Nutrasweet, Arthrotec, and the CMC CTD Global registration submission and approval for Telavancin ( Vibativ ) a peptide antibiotic. His academic work includes an adjunct professorship at St. John's University, College of Pharmacy and Allied Health Professions.
"About the title" may belong to another edition of this title.
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