BOULDER, Colo., May 29, 2019 /PRNewswire-PRWeb/ -- The Boulder Medical Device Accelerator program of Boulder iQ will participate in the 2019 Redefining Early Stage Investments (RESI) conference June 3 in Philadelphia.
Jim Kasic, general partner of the accelerator (BMDA), will be onsite to talk with companies that are seeking product development, quality and regulatory services, expert mentoring and infrastructure support in exchange for an equity investment from Boulder iQ, where Kasic also serves as president and CEO. Boulder iQ is an expert contract consulting firm that offers design engineering, development and turnkey manufacturing for consumer, high-technology and medical products, and complete regulatory, clinical and quality compliance services for medical device and in vitro diagnostic companies.
More than 700 fundraising executives, entrepreneurs, healthcare investors and strategic partners, and 100 service providers will attend the RESI conference, which provides an international venue for early-stage life science companies in the drug, medical device, diagnostics and digital health industries to source investors from around the globe, create relationships, and potentially, secure funding. The conference will include early-stage companies through those in the venture stage: companies seeking grants, seed, angel, series A and series B funding.
"The Boulder Medical Device Accelerator represents one of a very few opportunities where start-up companies in the healthcare industry can find full concept-though-manufacturing support," explains Kasic. "RESI offers a dedicated venue for us to identify companies that are looking to move their core technology to commercialization, and need agile product development services, expert mentoring and infrastructure support to do so."
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.
SOURCE Boulder iQ
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