Jesse Hart, MS, PMP
Jesse anchors the GRC and framework credibility behind this work. He brings 27 years across regulated industries including pharmaceutical, biotech, medical device, regulated software, clinical trials, healthcare technology, and financial services. His background includes FDA 21 CFR Part 11, HIPAA, GDPR, ISO 9001, ISO 27001, consent decree remediation, quality systems, vendor risk, AI governance, ISO 42001, NIST AI RMF, and evidence-ready compliance programs. For Pulse Governance, Jesse advises on diagnostic methodology, framework claim boundaries, field-level evidence requirements, finding structure, and the practitioner language needed for regulated buyers.
