Since the European Union (EU) General Data Protection Regulation (GDPR) became applicable on May 25, 2018, data protection regulators from the EU member states — gathered in the European Data Protection Board (EDPB) — have issued GDPR-focused opinions and recommendations at an increasing rate. With the GDPR being general in scope and industry-neutral, the EDPB quickly recognized that businesses require hands-on guidance on how to apply the new rules. Also, the ambiguity surrounding many provisions of the GDPR has triggered public demand for regulatory clarification, not in the least from life sciences companies.

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Disputes over medtech contracts are disruptive and costly. Dorothee Schramm, a partner at Sidley who concentrates in international commercial disputes, provides tips on how to save time and money in managing contract conflicts.

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State Comprehensive Privacy Bill Loses Steam, Data Breach Law Amendment Heads to Governor’s Desk","Target":"_blank","CssClass":"","Language":"","Children":null},"TemplateID":"dd10cce2-481e-48fe-a922-af8e2618d0a6"},{"ID":"82c7e883-dcad-4886-adf8-b4e3bde2facd","ContentType":"Sidley Updates","DisplayDate":"Spring 2019","Title":"Securities Class Actions in the Life Sciences Sector","ShortTitle":"","Summary":"

Sidley is pleased to present its annual year-in-review addressing developments in securities class actions brought against life sciences companies in 2018.

In this publication, we provide an overview and analysis of trends in decisions involving life sciences companies with products at two distinct stages of development—pre- and post-FDA approval. We also summarize each of the reported federal decisions in this area and catalog the new securities class action complaints filed against life sciences companies in 2018.

Click here to view a two-page summary.

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