Automation of the Design Control process can help product development teams navigate mandatory FDA regulations for medical device design controls. By making this process easier and more efficient, innovative medical devices can get to market quicker thereby having a greater impact of people’s lives. Tietronix Software has developed a Medical Device Accelerator (MDA), a web based system that includes design control, document control, CAPA and MDR reporting features. The MDA can benefit start-up companies by offering a “cafeteria” style plan, where a company can choose only the processes required at their stage of development. Click on MDA to read the entire article in Medical Design Briefs.
About UsOMEDtech, provides quality system design, regulatory, compliance, clinical and operations consulting services that are focused on helping managers and companies meet the aggressive challenges of bringing new medical device products to market.
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