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Gezondheidsrecht

R.B.M. Keurentjes, B.J.M. Frederiks, A.J.K. Hondius, I.M. Koopmans

Sdu Commentaar Gedwongen zorg - Editie 2021

Sdu Commentaar Gedwongen zorg bevat praktisch en diepgaand commentaar op artikelen uit de Wet verplichte ggz en de Wet zorg en dwang.
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Jolande Janssen
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Kees Wessels
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J.K.M. Gevers, E.J.C. de Jong, Johan Legemaate

Handboek Gezondheidsrecht

Deze achtste druk van Handboek gezondheidsrecht bevat een uitgebreide analyse van alle belangrijke thema’s binnen het gezondheidsrecht.
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paperbackEngels2014
This book is the first major work that addresses a core question in biomedical research: the question of acceptable risk. The acceptable level of risks is regulated by the requirement of proportionality in biomedical research law, which state that the risk and burden to the participant must be in proportion to potential benefits to the participant, society or science.  Meer
165,33
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paperbackEngels2013
whether the patient is suffering? Should the ability to think and reason be considered as the most important factor? For instance, should a patient with Amyotrophic lateral sclerosis (ALS) who is mentally alert yet unable to move from the neck down be allowed to refuse medical treatment; and, if so, at what point in her treatment should one consider her life no longer worth living?  Meer
105,63
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paperbackEngels2012
At a time when it is becoming usual for medicines to be developed for a global market and pharmaceutical companies are endeavouring to expedite the drug development process, Regulatory Authorities are concentrating on improving their efficiency and effectiveness.  Meer
86,01
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paperbackEngels2012
Considerable investment has been made by both pharmaceutical and biotechnology companies in pharmaceutical products of biotechnology. However, because relatively few of these products have been marketed, lack of relevant experience means that uncertainty still surrounds the most appropriate strategy for their safety evaluation.  Meer
157,95
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paperbackEngels2011
As 1992 looms on the horizon and preparation is made for the completion of the internal market in Europe, the CMR realised the value of addressing some of the issues involved and defining the objectives and achievements of medicines regulations in a number of EEC countries in comparison with Japan and the USA.  Meer
118,71
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paperbackEngels2011
Regulatory review is the last major development hurdle that must be passed by a new medicine before it reaches the market. At a time when pharmaceutical companies are reviewing their R&D strategies, and attempting to reduce drug development times, it is extremely important that the review process is made as efficient as possible.  Meer
171,03
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paperbackEngels2012
The Medicines Act 1968 together with its delegated legislation comprehensively controls the manufacture, packaging, labelling, distribution and promotion of medicines for both human and animal use in the United Kingdom.  Meer
114,78
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gebondenEngels2015
Biobank research and genomic information are changing the way we look at health and medicine. Genomics challenges our values and has always been controversial and difficult to regulate.  Meer
141,85
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PaperbackEngels2019
Explores relevant social issues related to various Chinese medicine treatments, including acupuncture and medicinal oils, as well as insight into practitioner licensing and public perception.  Meer
65,57
Verwachte levertijd ongeveer 6 werkdagen
gebondenEngels2017
This book offers all countries a guide to implementing verification systems for medical devices to ensure they satisfy their regulations. It describes the processes, procedures and need for integrating medical devices into the legal metrology framework, addresses their independent safety and performance verification, and highlights the associated savings for national healthcare systems, all with the ultimate goal of increasing the efficacy and reliability of patient diagnoses and treatment.  Meer
144,87
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paperbackEngels2018
The general scope of the book is the patentability and morality of human embryonic stem cell research in US, EU and China. The book observes fraudsters operate unsafe human embryonic stem cell therapies and officialdom turns a blind eye to the immoral human embryonic stem cell research in China.  Meer
184,11
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gebondenEngels2018
This book examines the position of children who provide tissue to potentially save the life of another. It questions whether child donors of all ages have been treated appropriately and whether they are sufficiently protected in acting as tissue donors, and ultimately considers whether a new regulatory response is needed to benefit donor children.  Meer
157,95
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paperbackEngels2018
This book examines the position of children who provide tissue to potentially save the life of another. It questions whether child donors of all ages have been treated appropriately and whether they are sufficiently protected in acting as tissue donors, and ultimately considers whether a new regulatory response is needed to benefit donor children.  Meer
112,17
Verwachte levertijd ongeveer 8 werkdagen
GebondenEngels
This book is intended to serve as a reference for professionals in the medical device industry, particularly those seeking to learn from practical examples and case studies.  Meer
140,16
Verwachte levertijd ongeveer 10 werkdagen

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