TRIADVI LLC · MICROSOFT 365 · DEVOPS · LIFE SCIENCES SERIALIZATION
Systems that hold up under audit, inspection, and examination.
We build and operate SharePoint, Power Platform, and DevOps environments — and the DSCSA serialization infrastructure that tracks a drug from the manufacturing line to the pharmacy shelf. Our clients answer to regulators, examiners, and the public, so what we ship has to be provable, not just functional.
Power Apps we build
Canvas apps, in productionRepresentative examples — the kind of purpose-built canvas apps we deliver to replace spreadsheet-and-email workflows with something your quality or ops team can stand behind.
What we build
Four disciplines, one standard of proof
Each practice stands on its own, and each one is built to the same requirement: every change is documented, every deployment is repeatable, and every claim about the system can be checked.
SharePoint & intranets
Modern SharePoint Online sites, document libraries, and intranet portals built for people who need to find the right version of a document under pressure — not browse a wiki.
- Information architecture & governance
- Modern page design & web parts
- Records retention & access control
Power Platform
Power Apps and Power Automate solutions that replace spreadsheet-and-email workflows with something your quality team can actually stand behind in an audit.
- Canvas & model-driven apps
- Automated approval & escalation flows
- AI Builder & Azure OpenAI integration
DevOps & release engineering
CI/CD pipelines and cloud infrastructure that make deployments boring — the way they should be for a system a bank or a state agency depends on.
- Pipeline design — GitLab CI/CD, Azure DevOps
- Container & Kubernetes deployment
- Monitoring, alerting & incident response
Pharmaceutical serialization
DSCSA-aligned track-and-trace: serialized packaging, EPCIS event data, and the SAP ATTP and middleware integrations that keep a product's history intact from line to dispense.
- Serialization & aggregation setup
- EPCIS event & trading-partner integration
- Validation documentation & SOP authoring
Who we build it for
Built for the industries with the highest bar for trust
State agencies, pharmaceutical manufacturers, and regulated banks share one thing: someone outside the organization is going to check the work. We design for that from day one.
State & government clients
Case management systems, internal portals, and workflow automation built to procurement standards and public-records requirements — not consumer-app conventions.
Top pharmaceutical manufacturers
DSCSA serialization, GxP-aware validation documentation, and SAP-integrated traceability for manufacturers who cannot treat compliance as an afterthought.
Regulated & secured banks
Internal tooling and platform work built around least-privilege access, audit logging, and change control that satisfies internal risk and external examiners alike.
How we work
A five-stage engagement, every time
The sequence doesn't change client to client. What changes is the depth at each stage, depending on how regulated the environment is.
Discover
We map the current system, its data flows, and — critically — who audits it and against what standard.
Architect
A design that names every integration point, every access boundary, and every piece of evidence the system will need to produce later.
Build
Implementation in version-controlled, peer-reviewed increments — deployed through the same pipeline every time, not by hand when convenient.
Validate
Test scripts, validation summaries, and SOP documentation written to the standard your quality or compliance function actually needs.
Sustain
Monitoring, incident handling, and periodic review, so the system that passed its first audit still passes its fifth.
Start a conversation
Tell us what has to hold up under review.
Whether it's a SharePoint migration, a DevOps pipeline, or a serialization program facing its first FDA inspection — bring us the system and the standard it has to meet.