Expert IoMT Analysis and Decision Support.
RoweBots provides independent technical leadership for investors, legal counsel, and IoMT medtech founders.
Three practices
Where deep IoMT expertise compounds.
Three decades of embedded systems, regulated software, and connected-device delivery — applied to the highest-stakes decisions in your organization.
VC Technical & Business Analysis
Rigorous technical due diligence and market validation for IoMT investments — from device architecture to regulatory exposure and competitive moat.
Learn moreExpert Witness for IoMT
Independent expert testimony and forensic analysis on connected medical device litigation, patent disputes, cybersecurity incidents, and standards-of-care.
Learn moreFractional CTO Services
Hands-on engineering leadership for connected medical device teams — architecture, IEC 62304, cybersecurity, FDA pre-sub strategy, and team scaling.
Learn moreIEC 62304
Medical device software lifecycle expertise across Class B/C systems.
ISO 13485 & 14971
Quality management and risk management across design, development, and post-market surveillance.
FDA, MDR & MDSAP
Pre-submission strategy, 510(k) technical files, EU MDR readiness, and MDSAP — covering FDA, Health Canada, Australia TGA, Brazil ANVISA, and Japan MHLW/PMDA.
UKCA & NICE
UK Conformity Assessed marking strategy and NICE Clinical Guidelines for Great Britain market access and evidence-based care pathways.
30+ yrs
Embedded, real-time, and connected-device engineering leadership.
Have an IoMT decision on the table?
Whether it's diligence on a $20M round, a deposition next quarter, or the architecture of your next connected device — let's talk.
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