This guide provides a compilation of insights from legal practitioners to assist in the understanding of regulations that impact the drug and medical device industry.
Topics covered include regulatory frameworks, manufacturing, transactions, advertising, promotion and sales, data privacy, product recalls, litigation, and dispute resolution.
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Region:
Global
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Australia
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Belarus
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Chile
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China
,
France
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Germany
,
India
,
Italy
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Japan
,
Peru
,
Poland
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Spain
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Switzerland
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Taiwan
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Turkey
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United Kingdom
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United States
The information in any resource collected in this virtual library should not be construed as legal advice or legal opinion on specific facts and should not be considered representative of the views of its authors, its sponsors, and/or ACC. These resources are not intended as a definitive statement on the subject addressed. Rather, they are intended to serve as a tool providing practical advice and references for the busy in-house practitioner and other readers.