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 19

EU, US regulators ease process for orphan drugs
  • Gowling WLG
  • USA, European Union
  • December 6 2007

In an effort to encourage development of drug treatments for rare diseases, the European Commission, the European Medicines Agency and the U.S. Food and Drug Administration announced steps to streamline the application process for orphan drugs.


Proposed legislation to regulate over-the-counter drug advertisements
  • Gowling WLG
  • USA
  • November 16 2007

New legislation has been introduced in response to the Food and Drug Administration (FDA) advisory on banning over-the-counter (OTC) cough and cold medicine.


Scott E. Foster
  • Gowling WLG

Mark Hines
  • Gowling WLG

Patrick Duxbury
  • Gowling WLG

Kieran Laird
  • Gowling WLG



Wendy J. Wagner
  • Gowling WLG