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Controlling and processing data in EU clinical trials
  • McDermott Will & Emery
  • European Union
  • November 22 2010

The legal regime for the conduct of clinical trials of medicinal products for human use in the European Union is set out in Directive 200120EC (the Clinical Trials Directive

The New EU Regulation on Medical Devices Aims at Enhanced Product Safety and Further Harmonization
  • McDermott Will & Emery
  • European Union, USA
  • May 9 2017

On May 5, 2017, the new Regulation on Medical Devices (MDR) and the new Regulation on In Vitro Diagnostics (IVDR) were published in the European

Focus on regulatory law - June 2014
  • McDermott Will & Emery
  • European Union, France
  • June 3 2014

If an appeal is lodged against an AMF decision to levy a financial penalty, the appeal judge has to verify that the penalty is proportionate in

International news: focus on compliance - winter 2014
  • McDermott Will & Emery
  • China, European Union, Germany, Global, USA
  • December 2 2014

As regulatory oversight of companiesfrom Sarbanes Oxley and the Dodd-Frank Act to the Foreign Corrupt Practices Act (FCPA) and the UK Bribery

Amy C. Pimentel
  • McDermott Will & Emery

Clive Stanbrook
  • McDermott Will & Emery

Frank Schoneveld
  • McDermott Will & Emery

Jenny J. Wang
  • McDermott Will & Emery

John Z.L. Huang
  • McDermott Will & Emery

Nathan Smith
  • McDermott Will & Emery