Boulder iQ, an expert product design and development consulting firm for the medical device and in-vitro diagnostic industries, will exhibit as an Emerging Tech partner at the 2019 American Medical Device Summit.
BOULDER, Colo. (PRWEB) October 24, 2019
Boulder iQ, an expert product design and development consulting firm for the medical device and in-vitro diagnostic industries, will participate in the 2019 American Medical Device Summit Oct. 28-29 in Chicago.
Boulder iQ will exhibit at Booth No. 3 as an Emerging Tech partner at the conference, taking place at the Hyatt Regency O’Hare. The company’s delegates to the summit include: Jim Kasic, president and CEO; Jeff Samson, strategy and planning specialist; Peggy Fasano, chief operating officer; and Carrie Hetrick, vice president of regulatory and clinical affairs.
The company’s executives will join 250 industry peers to review challenges and opportunities in medical device design, innovation, regulatory harmonization, compliance and digital transformation. Boulder iQ specializes in regulatory, quality and clinical compliance services for medical device and in-vitro diagnostic companies, and design, development and manufacturing for medical device products.
“The Summit offers a tremendous opportunity for leaders in the industry to share best practices and developing technologies in areas ranging from product development to post-market surveillance,” says Kasic. “Thought leaders come together to discuss the issues transforming our industry, including public policy on global market expansion and competitiveness, value-based health care and the impact of the EU MDR’s clinical evaluation reports. The venue is a perfect fit for Boulder iQ to leverage its approach to, and capabilities in, product design and development.”
About Boulder iQ (http://www.boulderiq.com)
Boulder iQ is an expert contract consulting firm offering design engineering, development and turnkey manufacturing for consumer, high-technology and medical products, and complete regulatory, clinical and quality management system services for the medical device and in-vitro diagnostic (IVD) industries. Based in Boulder, Colorado, the company is ISO 13485:2016 certified through Boulder BioMed.
The company’s Boulder Medical Device Accelerator provides an equity investment in start-up companies seeking product development services, expert mentoring and infrastructure support.
Contact: Aimee Bennett, Fagan Business Communications, 303-843-9840, email@example.com