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As devices get more connected and more capable, developing them becomes more complex. In this blog we share an overview of four key areas — UX/UI design, software development, regulatory compliance, and medical-software cybersecurity — and offer effective processes and best practices to follow as you work toward medical device certification. Thoughtful Design, Meticulous Development […]
Lisa cofounded R&Q in 2008, which was rebranded to RQM+ in 2020. As a member of the board of directors and executive leadership team, Lisa supports strategic planning and execution, and provides guidance across the company. Lisa leads the RQM+ Marketing Team, focusing on creating and executing innovative marketing strategies to profitably increase revenue and grow the brand. […]
How effective and early medical device strategy development can optimize your design and development process Written By: Marianna Gofman, Senior Consultant, IQVIA MedTech Regulatory Solutions Europe While continuous innovation supports new product design and development, it’s no wonder the healthcare industry is pressuring medical device companies to increase safety and efficiency, while also being innovative […]
Having partnered with MedTech and healthcare clients for over 30 years, we know how important new product launches are in this space. The stakes are high, and there’s enormous pressure to succeed At the same time, success isn’t easy to achieve: For instance you may be: Launching into a crowded, commoditized category Up against an […]
The Québec Government has partnered with the Medical Alley Association to deliver a customized U.S. go-to-market program for Québec companies in med-tech and digital health fields. The program, starting April 2021, will advance Québec’s and Medical Alley’s positions as global healthcare hubs. Québecis a world-renowned innovation center with a fast-growing health-technology cluster. The region is […]