<h1 class="entry-title">Category: Canada</h1>

Health Canada intends to adopt GHTF Summary Technical Documentation (STED) format for class III and IV device applications

August 2009 The Therapeutic Products Directorate (TPD), Health Canada has announced that it intends to adopt the Global Harmonization Task Force’s STED guidance document published February 21, 2008 to encourage and support the global convergence of documentation requirements for medical devices.  Adoption of the STED as a basis for demonstrating conformity to the Essential Principles […]