We use cookies to customise content for your subscription and for analytics.
If you continue to browse Lexology, we will assume that you are happy to receive all our cookies. For further information please read our Cookie Policy.

Search results

Order by: most recent most popular relevance



Results:1-10 of 23

Justice Department Outlines Factors That May Lead to Dismissal of More False Claims Act Cases
  • Greenberg Traurig LLP
  • USA
  • February 7 2018

An internal memo made public last month indicates that the U.S. Department of Justice (DOJ) may be moving to dismiss more False Claims Act (FCA) cases


Brexit: International and EU Legal Frameworks Affected and Unaffected
  • Greenberg Traurig LLP
  • USA, United Kingdom, OECD, European Union, Global
  • August 1 2016

This note identifies those European and international legal frameworks that are unaffected by Brexit and those that may cease to apply in the UK when


M&A, investment or partnering checklist for medtech companies
  • Greenberg Traurig LLP
  • USA
  • February 18 2015

Emerging medical device companies should consider these points when weighing a potential merger, strategic partnership or investment: 1. Identify


FDA issues draft guidances aimed at reducing oversight of low risk general wellness products and medical device accessories
  • Greenberg Traurig LLP
  • USA
  • January 30 2015

On Jan. 20, 2015, the U.S. Food & Drug Administration (FDA) issued two anticipated draft guidance documents proposing reduced FDA oversight of two


CFDA seeks comments on revised draft of the Measures on the Administration of the Standards of Medical Devices
  • Greenberg Traurig LLP
  • China
  • January 20 2015

On Oct. 24, 2014, the China Food and Drug Administration (the CFDA) released for public comments the proposed draft of the revised Measures on the


National Food and Drug Administration publishes newly modified measures regarding medical devices
  • Greenberg Traurig LLP
  • China
  • October 27 2014

On July 30, 2014, the National Food and Drug Administration released newly modified Administrative Measures for the Registration of Medical Devices


China life science laws and regulations update
  • Greenberg Traurig LLP
  • China
  • July 15 2013

To deepen Government Reform and improve government efficiency and transparency, the State Council of the People's Republic of China recently released


Twelfth Five-Year (2011-2015) plan for medical device and equipment industry
  • Greenberg Traurig LLP
  • China
  • April 2 2012

The PRC Ministry of Science and Technology (MOST) issued the Twelfth Five-Year (2011-2015) Specific Plan for Medical Device and Equipment Industry (the “Medical Plan”) on January 19, 2012.


Food exports allowed to Iran and Sudan under new General License
  • Greenberg Traurig LLP
  • USA, Sudan, Iran
  • October 17 2011

On October 12, 2011, the U.S. Treasury Department's Office of Foreign Assets Control (OFAC) issued two important General Licenses (GLs) authorizing the export and reexport of “food” to Iran and Sudan, respectively.


EU court judgment may add 6.5 percent customs
  • Greenberg Traurig LLP
  • European Union
  • July 13 2011

A recent case at the European Court of Justice can have important consequences for imports of accessories and disposables for medical devices, as these may be subject to a customs tariff of 6.5 percent.