Is Agnotic a Sprinto partner?

This page does not describe a partnership. Agnotic Technologies is a software development services company: we build the product controls and connect them to the compliance platform you have chosen. Ask Sprinto directly about its partner and auditor programs.

What should we confirm with Sprinto before we start?

Which of your systems it connects to directly, what evidence format it accepts for custom systems, how it handles product-level audit logs, whether any connector could see PHI and what agreement covers that, and which frameworks you will run on it. We plan the build from the vendor's answers.

Should the compliance platform ever see PHI?

We design it so it does not. Connectors read configuration, user lists and log metadata, not patient records. Where a log line could contain PHI, we remove or tokenize it before export.

How long must HIPAA compliance documentation be kept?

The Security Rule requires its documentation to be kept for six years from the date it was created or last in effect, whichever is later (45 CFR 164.316(b)(2)(i)). We set retention on evidence exports and logs to match your policy.

Can the same evidence support a SOC 2 audit?

Much of it can, because access reviews, change records and backups appear in both. A SOC 2 report is issued by a CPA firm on your controls, so the auditor decides which evidence it accepts.

How long does an evidence integration project take?

It depends on scope; we agree a fixed first release on the scoping call. A product that already logs access events needs less work than one where audit logging has to be built first.

Do you sign a BAA for this work?

Yes. Agnotic signs a business associate agreement before any PHI is shared, and evidence work uses configuration and metadata, not patient data.

Compliance lead and software engineer at a table in a quiet office, reviewing a printed audit checklist beside an open laptop

Sprinto Healthcare Compliance

Engineering Evidence for Sprinto Healthcare Compliance

Your compliance platform is set up, but its controls stay open until the product itself produces the evidence. Agnotic Technologies builds access reviews, audit logs, change records and backup tests into your healthcare product, then connects them to a compliance automation platform such as Sprinto.

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What engineering evidence does Sprinto healthcare compliance need?

Sprinto healthcare compliance work depends on evidence from the product itself: access reviews, audit logs, change records, a vendor and BAA list, and tested backups. Agnotic Technologies builds those controls into your healthcare product and connects its systems to the compliance automation platform, so the evidence is produced by the software rather than assembled by hand.

Which evidence must your product produce?

A compliance automation platform reads evidence from the systems you connect to it. These are the eight items we make sure a healthcare product produces, accurately and in a form the platform can read. We confirm each connector and evidence format with the vendor at scoping.

Access reviews

Who can reach ePHI, by role, exported from your identity provider and the product's own admin roles, with leavers removed. HIPAA asks for access authorization and termination procedures (45 CFR 164.308(a)(3) and (a)(4)).

Audit logging

Product logs of who viewed or changed which record and when, kept tamper-evident. The Security Rule requires audit controls and regular review of activity records (45 CFR 164.312(b) and 164.308(a)(1)(ii)(D)).

Change management

Every production change traced from ticket to pull request, review, test run and deploy, so the platform can show each change was approved.

Vendor and BAA list

Every vendor that touches PHI, with its BAA status, hosting region and the data it receives. HIPAA requires business associate contracts for these vendors (45 CFR 164.308(b)).

Backups and restore tests

Automated backups of ePHI with scheduled restore tests and recorded results. HIPAA requires a data backup plan and a disaster recovery plan (45 CFR 164.308(a)(7)).

Encryption settings

Encryption for storage, databases and transport, exported as configuration the platform can read rather than as screenshots.

Vulnerability and dependency scans

Scan results from the build pipeline and cloud account, with each fix linked to its ticket.

Risk analysis inputs

A system inventory and data-flow map that feed your documented risk analysis, which the Security Rule requires (45 CFR 164.308(a)(1)(ii)(A)).

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How we connect it

How does Agnotic wire your product into the platform?

Four steps. The platform tracks the controls; we make sure the product and its systems can prove them.

Map controls to systems

For each control the platform tracks, we name the system that proves it: cloud account, identity provider, code repository, ticketing or the product database.

Close gaps in the product

We build what is missing in the software itself: audit events, role exports, backup jobs and restore tests.

Connect and check evidence

We use the platform's own connectors where they exist, or export evidence in the format the vendor documents, then check every control reads correctly.

Keep it current

Evidence checks run in the release pipeline, so a new service, vendor or role shows up before an audit does.

Sprinto healthcare compliance FAQs

No. A platform such as Sprinto tracks controls and collects evidence, but the safeguards have to be built into the product, and your team still owns the risk analysis, policies and BAAs. There is no official HIPAA certification; the Security Rule requires a documented risk analysis instead (45 CFR 164.308(a)(1)(ii)(A)).

Build compliantly

How we deliver on this standard