Recent Articles

November 6, 2017 8:41 am
Matthew M. Lowe
The MDR is a 306-page document consisting of 10 chapters and16 annexes ...
October 26, 2017 3:17 pm
Nina Passoth, Life Sciences Communications (Berlin, Germany)
MEDICA ACADEMY offers the latest expertise and practical tips on implementation of infection prevention for hospital and practice scenarios ...
October 25, 2017 8:46 am
Richard Hausmann, CEO, Elekta
Today, the use of 3D grids to localize tumors, mechanical advances that enable more precise shaping of radiation beams ...
October 20, 2017 8:25 am
Francisco Almada Lobo, CEO, Critical Manufacturing
More than any other industry, the production of medical devices demands the highest quality levels ...
October 9, 2017 8:39 am
Alex Butler, Manager of Medical Device Solutions, MasterControl
The process for obtaining a device clearance or premarket approval (PMA) in the United States is not the same as applying for a Shonin in Japan or a CE mark in Europe, but the challenges are similar ...
October 2, 2017 8:37 am
Alex Butler, Manager of Medical Device Solutions, MasterControl
Whether your company is developing a new and innovative device or re-launching an iterative product the key to a timely and successful regulatory submission is effective dossier management ...
September 29, 2017 8:45 am
Joe Reynolds, Research Manager at Noble
To accurately represent the real device, trainers not only need to address a device’s speed control, but also all functions that require force application by the patient ...
Subscribe to Medical Design Technology