Re-engineering clinical trials : best practices for streamlining the development process /

The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Enginee...

Descripción completa

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Sch�uler, Peter, Buckley, Brendan
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam : Academic Press, 2015.
Temas:
Drugs > Testing.
Drug development > Safety measures.
Clinical trials.
Drug development > Economic aspects.
Drugs > Design.
Clinical Trials as Topic
Drug Approval
Drug Design
M�edicaments > Essais cliniques.
M�edicaments > D�eveloppement > S�ecurit�e > Mesures.
�Etudes cliniques.
M�edicaments > D�eveloppement > Aspect �economique.
M�edicaments > Conception.
MEDICAL > Pharmacology.
Drugs > Design
Clinical trials
Drugs > Testing
Acceso en línea:Texto completo
Descripción
Sumario:The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Engineering Clinical Trials evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and ...
Descripción Física:1 online resource (383 pages) : illustrations (some color)
Bibliografía:Includes bibliographical references and index.
ISBN:9780128007907
0128007907

Ejemplares similares