Posts Tagged ‘ Patient registry ’

Netherlands Newspaper Investigates Mesh Mess

Dec 29th, 2011 | By
Netherlands Newspaper Investigates Mesh Mess

DECEMBER 29,  2011 ~ The Netherlands will begin a patient registry of synthetic gynecological mesh in early 2012 requiring gynecologists to report the growing number of complications emerging from use of the mesh.  The U.S. has yet to establish post-surgery patient tracking to determine the actual number of adverse events.  Investigative reporter, Ellen de Visser
[continue reading...]



We hope you find this a helpful resource. National News Editor, Jane Akre, began MDND with the hope of providing the latest news, information and perspective from the regulatory, industry and patient point of view, something that goes under-reported in much of the coverage of medical devices. The public is just now becoming aware that many devices do not undergo the same scrutiny as prescription drugs and are instead grandfathered in under an FDA loophole that has gone largely unchanged since the 1970s. As a result, patients become the post-market clinical trial subjects, and many suffer devastating and permanent injuries.