Boulder iQ Highlights Product Development Support at RESI Conference

-- Industry leader supports life science developers --

BOULDER, Colo., June 4, 2025 /PRNewswire/ -- Boulder iQ will exhibit at the 2025 Redefining Every Stage of Investment (RESI) conference June 16 in Boston.

As an expert contract consulting firm, Boulder iQ provides full, integrated services that life science developers need to bring their product to market: product design and development, regulatory and quality, manufacturing and assembly, sterilization, and packaging and labeling.

"We're a strategic partner in the business of helping early-stage companies speed their products to market," explains Jim Kasic, president and CEO of Boulder iQ. "When companies get the funding they need to forward, we are able to help them navigate the complex development processes – and do so quickly, cost-effectively and successfully."

Several hundred investors and strategic partners will take part in the RESI conference series, which connects early-stage life science and healthcare companies with investors and strategic partners. Start-up companies can source funding and build relationships, ultimately aiming to get funding and support for their early-stage projects. 

"The industry offers very few opportunities for early-stage companies can find full concept-though-manufacturing support with experienced experts," 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 support to do so." 

Boulder iQ (www.boulderiq.com)

Boulder iQ is an expert contract firm that provides life sciences companies all the services they need to bring products to market. Sister companies Boulder Sterilization and Boulder Regulatory Affairs and Quality Assurance work together to help developers speed products to market. Boulder Sterilization provides quick-turn ethylene oxide (EO) and chlorine dioxide (CD) sterilization services for medical devices and in-vitro diagnostic products. Boulder Regulatory Affairs and Quality Assurance provides full regulatory and quality support.

Based in Boulder, Colorado, Boulder iQ is ISO 13485:2016 certified through Boulder BioMed.

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SOURCE Boulder iQ