By Stewart Eisenhart, Emergo Group
Ensuring safe and effective use of medical devices for patients and users is a crucial responsibility for manufacturers and developers, not only in terms of addressing regulatory requirements but also of mitigating risks to public health. In order to pass scrutiny from market regulators and demonstrate that their products do not compromise public health and trust, medical device and technology companies must tie safety and risk management processes closely to their design, development and pre- and post- commercialization efforts.
Get the full story here at the Emergo Group’s blog.
The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MedicalDesignandOutsourcing.com or its employees.