Medical companies across different stages, from early development through commercialization. This includes startups and growing teams, as well as more established organizations that need flexible regulatory and quality support, whether for specific projects or to complement internal capabilities.

Most work is done remotely, with on‑site support available in the San Francisco Bay Area.

Yes. My primary focus is on hands-on implementation and documentation support. In certain cases, I can provide input or support on regulatory or quality‑related decisions, working alongside internal teams or existing leadership.

Yes. Support can be extended as needed, but engagements are intentionally structured to avoid long‑term hiring commitments. Scope and duration are defined based on current needs and priorities.

Engagements are flexible and can be structured on an hourly, part-time, or project basis, depending on the scope and duration of the work. Details are discussed during the initial conversations.

We start with a free initial consultation to discuss your needs, scope, and timelines. This call also helps confirm that my experience is a good fit for your project. If aligned, support is formalized with the appropriate agreements and structured to fit your team and objectives.

Engagements are typically project‑based or temporary. This can include short‑term support for a defined project, fractional or hourly support over a period of time, or recurrent assistance during peak workload phases such as submissions, audits, or remediation activities.