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Biomedical Product Development: Bench to Bedside

Engelsk Paperback
SPAR
kr 150

Biomedical Product Development: Bench to Bedside

Engelsk Paperback

This textbook covers all the steps in manufacturing a biomedical product from bench to bedside. It specifically focuses on quality assurance and management and explains the different good practice principles in the various phases of product development as well as how to fulfill them: Good laboratory practice, good manufacturing practice and good clinical practice.  

It provides readers with the know-how to design biomedical experiments to ensure quality and integrity, to plan and conduct standard preclinical studies and to assure the quality of the final manufactured biomedical products.  Importantly, it also addresses ethical concerns and considerations.

The book discusses the guidelines and ethical considerations for preclinical and clinical studies, to allow readers to identify safety concerns regarding biomedical products and to improve pre-clinical studies for the development of better products.

This textbook is a valuable guide for biomedical students (B.Sc., M.S., and Ph.D. students) in the field of molecular medicine, medical biotechnology, stem cell research and related areas, as well as for professionals such as quality control staff, tissue bankers, policy-makers and health professionals.


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This textbook covers all the steps in manufacturing a biomedical product from bench to bedside. It specifically focuses on quality assurance and management and explains the different good practice principles in the various phases of product development as well as how to fulfill them: Good laboratory practice, good manufacturing practice and good clinical practice.  

It provides readers with the know-how to design biomedical experiments to ensure quality and integrity, to plan and conduct standard preclinical studies and to assure the quality of the final manufactured biomedical products.  Importantly, it also addresses ethical concerns and considerations.

The book discusses the guidelines and ethical considerations for preclinical and clinical studies, to allow readers to identify safety concerns regarding biomedical products and to improve pre-clinical studies for the development of better products.

This textbook is a valuable guide for biomedical students (B.Sc., M.S., and Ph.D. students) in the field of molecular medicine, medical biotechnology, stem cell research and related areas, as well as for professionals such as quality control staff, tissue bankers, policy-makers and health professionals.


Produktdetaljer
Sprog: Engelsk
Sider: 157
ISBN-13: 9783030356255
Indbinding: Paperback
Udgave:
ISBN-10: 3030356256
Udg. Dato: 6 feb 2020
Længde: 0mm
Bredde: 240mm
Højde: 168mm
Forlag: Springer Nature Switzerland AG
Oplagsdato: 6 feb 2020
Forfatter(e):
Forfatter(e)


Kategori Farmaceutisk kemi og teknologi


Sprog Engelsk


Indbinding Paperback


Sider 157


Udgave


Længde 0mm


Bredde 240mm


Højde 168mm


Udg. Dato 6 feb 2020


Oplagsdato 6 feb 2020

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