Our client, a global contract manufacturer, was expanding their engineering capabilities into the medical device industry and lacked the experience to develop software in accordance with IEC 62304 required for FDA approval. In a risk assessment, their end customer had rated software as the highest risk component of the overall development and manufacturing effort.
Randstad Engineering Solutions was able to leverage its decades of experience in the development of safety-critical software to bring leadership and guidance to our customer in completing the software per the applicable standards. Key elements of our solution included:
Randstad Engineering Solutions was able to help our client meet and exceed their customer's expectations, including: