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Regulated use cases

Deep experience where control matters.

doss serves organizations across industries. We bring particular depth to healthcare, life sciences and other regulated or high-control processes where documentation, testing, validation and governance are part of the solution—not an afterthought.

Regulated & high-risk work

A specialty built from direct experience—not a limit on who we serve.

doss's deepest experience in regulated automation comes from healthcare and life sciences, including GxP use cases. That background shaped a core principle: accelerating application development does not create much value if documentation, testing, validation and governance remain disconnected from the way the solution is built.

doss applies the same process-first automation approach across industries. This page simply highlights the additional experience we bring when quality, security, compliance or operational risk require a more deliberate control model.

Quality & validation framework

Adapt the control framework to the technology.

For regulated applications, doss can help define documentation structures and validation approaches that reflect the reusable nature of modern application platforms. In life-science environments, that can include artifacts such as user requirements, solution/design documentation and IQ/OQ protocol formats.

Reusable documentation

Structure requirements, design information and testing so common platform capabilities do not have to be rediscovered and re-documented from scratch for every application.

Risk-based controls

Match the level of documentation, testing, approval and governance to the risk and intended use of the solution rather than applying the same treatment indiscriminately.

Validation automation

Automation should also improve the work around software delivery.

When applications can be designed and changed quickly, quality processes can become the new bottleneck. doss looks for opportunities to use native platform and integration capabilities to automate supporting activities such as document generation, protocol creation, change-management records and approval workflows.

Citizen & distributed development

Give domain experts more capability without abandoning governance.

No-code/low-code and AI-assisted development can move solution creation closer to the people who understand the process. In regulated environments, however, decentralization needs a deliberate control model. doss uses risk-based approaches to identify where distributed development is appropriate and how capabilities can be introduced in phases.

Direct experience

Where doss's regulated perspective comes from.

Healthcare & life sciences

doss was created after applying modern application-platform technology to business processes in life-science organizations and confronting the documentation, validation and quality requirements that come with those environments.

GxP and non-GxP use cases

The original doss work included both regulated and non-regulated business applications, which reinforced the need to scale controls to the risk of the specific use case.

End-to-end SDLC support

doss can support design, documentation, development, testing, validation and support as one lifecycle or integrate with a customer's existing responsibilities and quality model.

Move quickly without pretending controls do not matter.