Author: Steven E. Linberg
Edition: 3
Publisher: Parexel Intl Corp
Binding: Paperback
ISBN: 188261576X
Expediting Drugs and Biologics Development: A Strategic Approach 2006
Using a unique reverse-engineering approach, dozens of leading experts with extensive experience in all disciplines of drug and biologic development show how careful planning and a sharp focus on the end-goals can be used to expedite even the most complex product development programs today! From the first preclinical testing to clinical trials to the NDA/BLA review, Expediting Drug and Biologics Development shows you how to use reverse-engineering techniques to drive and improve each aspect of a development program's design and implementation. Medical books Expediting Drugs and Biologics Development. The new third edition of Expediting Drug and Biologics Development is not a summary of U.S. or international regulatory requirements. Rather, it is a real-world doer's guide to drug and biologics development Medical books New Drug Approval Process: Accelerating Global Registrations Drugs And The Pharmaceutical Sciences Volume 139. New York: Marcel Dekker 2004. Book. Very Good Ex-Library Cond Book. Hardcover. 4th Edition; minimal Library Markings. 8vo - over 7¾" - 9¾" tall. 635 pgs. Covers: reguklatory practices and procedures of new drug biologic and device development; clinical research development; specific aspects in the process of new product submissions; global applications of good clinical practices; effective and new methodologies in expediting new product approvals in the US and EU. Maroon/white glossy boards. Minimal library markings; no card pocket. Clean and tightly bound.
Download link for Expediting Drugs and Biologics Development : A Strategic Approach 2006
New York: Marcel Dekker 2004. Book. Very Good Ex-Library Cond Book. Hardcover. 4th Edition; minimal Library Markings. 8vo - over 7¾" - 9¾" tall. 635 pgs. Covers: reguklatory practices and procedures of new drug biologic and device development; clinical research development; specific aspects in the process of new product submissions; global applications of good clinical practices; effective and new methodologies in expediting new product approvals in the US and EU. Maroon/white glossy boards. Minimal library markings; no card pocket. Clean and tightly bound.
This book is a proceedings of the AAPS Stability Workshop. This workshop provide an understanding of the regulatory perspective of Stability Testing and position the stability program for 21st century globally by: Learning regulatory initiatives on global stability submission.Stability testing in challenging storage environment such as ASEAN or Caribbean region.Exploring concept of Quality by Design as it applies to stability testing.Understanding stability challenges of biologics, generics, nutraceutical, and other new product technology.Setting specifications for Drug Substances as well as v
This book is a proceedings of the AAPS Stability Workshop. This workshop provide an understanding of the regulatory perspective of Stability Testing and position the stability program for 21st century globally by:
Learning regulatory initiatives on global stability submission.
Stability testing in challenging storage environment such as ASEAN or Caribbean region.
Exploring concept of Quality by Design as it applies to stability testing.
Understanding stability challenges of biologics, generics, nutraceutical, and other new product technology.
Setting specifications for Drug Substances as well
Learning regulatory initiatives on global stability submission.
Stability testing in challenging storage environment such as ASEAN or Caribbean region.
Exploring concept of Quality by Design as it applies to stability testing.
Understanding stability challenges of biologics, generics, nutraceutical, and other new product technology.
Setting specifications for Drug Substances as well
This book is a proceedings of the AAPS Stability Workshop. This workshop provide an understanding of the regulatory perspective of Stability Testing and position the stability program for 21st century globally by: Learning regulatory initiatives on global stability submission.Stability testing in challenging storage environment such as ASEAN or Caribbean region.Exploring concept of Quality by Design as it applies to stability testing.Understanding stability challenges of biologics, generics, nutraceutical, and other new product technology.Setting specifications for Drug Substances as well as v
Medical Book Expediting Drugs and Biologics Development
The new third edition of Expediting Drug and Biologics Development is not a summary of U.S. or international regulatory requirements. Rather, it is a real-world doer's guide to drug and biologics development. It provides dozens of templates, forms, and tools to assists those in the trenches of new drug and biologic development today. With this book, you will learn how to: * Apply the very latest and most advanced project management techniques directly to challenges presented by the drug development process. * Critically evaluate the needs of the package insert and marketing application up front, before getting deeply into clinical trials. * Leverage standardization to drive and expedite the entire development process, from the development of clinical trial protocols to the development of clinical data presentations. * Critically assess the needs of the final report before developing the clinical protocol. * Use draft case report forms (CRF) to dictate the content of the procedures section of the clinical protocol. * Constructively consider the methods for data analysis in developing the clinical protocol. In addition, Expediting Drug and Biologics Development 2006 will provide you with direct access to the expertise and recommendations of dozens of the most experienced and forward-thinking experts in the pharmaceutical and biotechnology industries today.
