Sunday, August 29, 2010

FDA Pre-Market Approval Workshops – Toronto & Montreal, Sept.21-23


Date: September 21 to 23, 2010
Location: Toronto and Montreal, Canada

Contact: Cynthia Stevenson, Trade Commissioner (Health Industries), Canadian Embassy, Washington, D.C.

Two specialists from the FDA’s Center for Devices and Radiological Health will present day-long workshops to Canadian manufacturers of medical devices and technologies and supporting institutional stakeholders that are approaching completion of product development with intent to export to the U.S. in the near term. The workshops address in-depth the requirements for Pre-Market Notification (510(k)) and Pre-Market Approval (PMA) procedures for the importation of medical devices and technologies into the U.S.