EU Pharmaceutical Legislation Handbook. Vol. 5 Stem Cell Reserch Legislation and Regulations (World Strategic and Business Information Library)

EU Pharmaceutical Legislation Handbook. Vol. 5 Stem Cell Reserch Legislation and Regulations

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Safety, Ethics and Regulations (Stem Cells in Clinical Applications)

This invaluable resource discusses the saftey, ethics, and regulations of developing stem cell clinical applications. Each chapter is contributed by a preeminent scientist in the field and covers such topics as clinical safety of stem cell gene therapy, the patentability of hESC technologies, international guidelines, challenges to international stem cell clinical trials, worldwide regulations including in emerging markets like China and Taiwan.


Saftey, Ethics, and Regulations  and the other books in the  Stem Cells in Clinical Applications  series will be invaluable to scientists, researchers, advanced students and clinicians working in stem cells, regenerative medicine or tissue engineering.

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Stem Cells and Good Manufacturing Practices: Methods, Protocols, and Regulations

This volume collects a series of protocols describing the kinds of infrastructures, training, and standard operating procedures currently available to actualize the potential of stem cells for regenerative therapies. Stem Cells and Good Manufacturing Practices: Methods, Protocols, and Regulations pulls together key GMP techniques from laboratories around the world. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.

Inclusive and authoritative, Stem Cells and Good Manufacturing Practices: Methods, Protocols, and Regulations will be an invaluable resource to both basic and clinical practitioners in stem cell biology.

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