Requirements-to-release for regulated patient and provider platforms
Full SDLC delivery across product, engineering, QA, and clinical stakeholders on FDA-regulated applications.
- Zero-downtimeMigration discipline
- Multi-stakeholderSDLC coordination
The challenge
Regulated patient and provider applications required rigorous requirements discipline, cross-functional coordination, and release management that could withstand clinical and compliance scrutiny—while still shipping on schedule.
Frame, ship, govern
- Frame
Led requirement gathering and SDLC planning across product, engineering, QA, and clinical stakeholders. Defined scope, release criteria, and adoption KPIs aligned to customer and regulatory expectations.
- Ship
Managed data and integration workstreams, zero-downtime migrations, and operational runbooks. Coordinated internal and external stakeholders through build, test, and release phases.
- Govern
Defined adoption and reliability KPIs, post-launch stabilization plans, and release management processes. Acted as primary liaison for scope, schedule, and readiness decisions.
Outcomes
- Delivered regulated patient and provider applications through full SDLC
- Achieved zero-downtime migration discipline on critical releases
- Established adoption and reliability KPIs with post-launch stabilization
- Maintained stakeholder accountability across clinical and technical teams
Practice areas
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