Varick's Agents get care authorized, claims paid, and every filing in on time.

With a scoped 4-week pilot on one high-volume workflow, often prior authorization or denials. Forward-deployed engineers mine the process from Epic or your claims system with read-only access, interview the team, read your payer policies, and baseline measures such as days to decision and initial denial rate.

Yes. Varick signs a BAA before any work touches protected health information, and agents get only the minimum necessary access for each workflow, under identities your team provisions.

No. Clinicians decide care, and utilization management nurses and medical directors decide medical necessity. Agents assemble the evidence, and no agent denies a request or a claim.

Under your own computer system validation or computer software assurance procedure. We write the risk assessment and the test evidence with your quality team, every model is benchmarked on the workflow before go-live, and every agent action is recorded in the system's audit trail under 21 CFR Part 11 controls.

Yes. For device makers the usual starting point is complaint handling and medical device reporting under 21 CFR 803. For biotechs still in the clinic it is site activation and the trial master file.

No. Agents run in your own cloud account, in the region you choose. Charts, claims, prompts, and logs stay inside your boundary, and none of it is used to train a model.