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This fresh and insightful Research Handbook delivers global
perspectives on information law and governance, delving into
principles of information law in the areas of trade secrecy,
privacy, data protection and cybersecurity. Providing US, Japanese
and European perspectives, this Research Handbook presents an
overview of legal regimes concerning the protection of information,
with a particular focus on trade secrecy protection. Top
international contributors offer analyses of general principles of
information law, rights in data, the tension between trade secrecy
and the freedom of information and the cross-fertilisation between
national and regional data protection regimes. Presenting an
interdisciplinary and holistic approach to information law and
governance, this innovative Research Handbook will be useful to
those researching trade secrets, privacy and data security laws.
The broad range of perspectives will also appeal to attorneys and
information professionals who are engaged in information governance
activities on behalf of their clients or employers.
Medicinal chemistry is both science and art. The science of
medicinal chemistry offers mankind one of its best hopes for
improving the quality of life. The art of medicinal chemistry
continues to challenge its practitioners with the need for both
intuition and experience to discover new drugs. Hence sharing the
experience of drug research is uniquely beneficial to the field of
medicinal chemistry. Drug research requires interdisciplinary
team-work at the interface between chemistry, biology and medicine.
Therefore, the topic-related series Topics in Medicinal Chemistry
covers all relevant aspects of drug research, e.g.
pathobiochemistry of diseases, identification and validation of
(emerging) drug targets, structural biology, drugability of
targets, drug design approaches, chemogenomics, synthetic chemistry
including combinatorial methods, bioorganic chemistry, natural
compounds, high-throughput screening, pharmacological in vitro and
in vivo investigations, drug-receptor interactions on the molecular
level, structure-activity relationships, drug absorption,
distribution, metabolism, elimination, toxicology and
pharmacogenomics. In general, special volumes are edited by well
known guest editors.
Medicinal chemistry is both science and art. The science of
medicinal chemistry offers mankind one of its best hopes for
improving the quality of life. The art of medicinal chemistry
continues to challenge its practitioners with the need for both
intuition and experience to discover new drugs. Hence sharing the
experience of drug research is uniquely beneficial to the field of
medicinal chemistry. Drug research requires interdisciplinary
team-work at the interface between chemistry, biology and medicine.
Therefore, the topic-related series Topics in Medicinal Chemistry
covers all relevant aspects of drug research, e.g.
pathobiochemistry of diseases, identification and validation of
(emerging) drug targets, structural biology, drugability of
targets, drug design approaches, chemogenomics, synthetic chemistry
including combinatorial methods, bioorganic chemistry, natural
compounds, high-throughput screening, pharmacological in vitro and
in vivo investigations, drug-receptor interactions on the molecular
level, structure-activity relationships, drug absorption,
distribution, metabolism, elimination, toxicology and
pharmacogenomics. In general, special volumes are edited by well
known guest editors.
For the first time, this book provides an up-to-date history of
product design and product design law covering 17 countries -
Japan, Korea, China, Singapore, the United Kingdom, Germany,
France, Italy, the Nordic countries (Denmark, Finland, Iceland,
Norway and Sweden), Russia, the United States, Brazil and Australia
- selected for their innovative or influential approach to design
or design protection. Each country is the subject of two chapters -
one on the history of design and the other on the history of design
law - authored by experts in design and intellectual property (IP)
law. This unique interdisciplinary approach explains why and how
various national design protection systems (that can include
design, copyright, trade mark, competition and civil laws)
developed, making it an ideal book for students, researchers and
lawyers. The book also serves as an international survey of
different national policy and legal responses to historical
developments and specific design and legal issues allowing readers
to consider their advantages and disadvantages - and so is also
recommended for policy and law makers, as well as organizations
that administer IP rights. Topics include the subject matter of
design protection; procedural and substantive requirements; design
registration; infringement; and the overlap of design rights and
other IP rights. The chapters on design history provide further
context to the historical development of these legal concepts by
considering major design movements, key designers and iconic
designs and the current state of design. The chapters highlight the
connected and often complementary relationship between the two
histories, not only for each country, but at the regional and
international level, often as a result of government policies,
trade, colonialism, immigration and globalisation. Design and
design practice continue to become more global and evolve with
developments in technology. At the same time, design laws are not
internationally harmonized and continue to develop at the national
level, with a number of significant changes occurring in recent
years. This timely book shows how the lessons of the past continue
to inform the future direction of design and the legal systems
developed to protect it.
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