Industry Partners

Greenlight Guru is the leading cloud-based platform that provides purpose-built for MedTech companies. The end-to-end solution streamlines product development, quality management, and clinical data management by integrating cross-functional teams, processes, and data throughout the entire product lifecycle. Greenlight Guru’s platform is used by organizations across the globe that are replacing their disjointed, legacy tools and solutions to bring life-changing products to people faster, and with less risk.

Match Health Collective is a full-service digital marketing agency focused on the healthcare industry. With expertise in content strategy, visual design, patient engagement, and digital marketing we drive growth by humanizing healthcare marketing.

Argenta Advisors™, Inc. is a recognized leader in the field of health policy and reimbursement for the life science industry.  Argenta provides a comprehensive range of healthcare and reimbursement consulting services throughout the medical technology lifecycle, from policy to practice.

Nocturnal Product Development is focused on helping early-stage companies accelerate device design, development, and commercialization. With unique expertise in class II and class III, implantable, and lifesaving devices, our result-based pricing allows you to plan your budget and reach your milestones with confidence.

Cooley is a premier full-service law firm for MedTech innovators and their investors. Our lawyers serve as strategic business partners to hundreds of MedTech companies around the world. With deep experience in this industry, we have access to leading venture capitalists, financial institutions and other strategic partners that support high-growth MedTech companies.

MedTech Impact Partners is led by Kwame Ulmer, a former FDA Director who spent over a decade evaluating medical technologies. MedTech Impact Partners assists MedTech companies from pre-series A to Fortune 500 and helps them get through the regulatory process and FDA.

Rook specializes in Quality and Regulatory strategies for early-stage medical device clientele, providing expertise in FDA regulations, MDSAP audits, ISO 13485:2016 compliance, and MDR conformity. Rook works with a wide range of devices, including class I-III devices, SaMD, and IVD.

MIDI is an award-winning strategic turnkey, FDA, and ISO compliant product development consulting firm with over 45 years of experience servicing domestic and international clientele representing medical, life sciences, and home healthcare markets.

Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment by offering expert guidance from concept through to commercialization and across the development continuum.

Virtonomy.io accelerates medical device development and clinical trials with an end-to-end digital twin and simulation solution based on an ever-expanding database of real clinical data to reflect anatomical variability, demographic diversity and pathological conditions.