iDaltu helps Public Sector and Life Sciences teams take control of regulated content—reducing risk, accelerating change, and improving user adoption across your ECM landscape.
Secure capture, controlled storage, lifecycle governance, inspection-ready audit trails, and search that works across regulated repositories
Modernisation, integration, upgrades, migration, and operating-model delivery—built for Life Sciences use cases (SOPs, QMS docs, submissions content, labeling, PV, training records).
A modern AI-driven platform that enhances discovery, extraction, summarisation, and secure distribution—without compromising governance
GxP validation pressure and audit readiness demands
Massive volumes of documents and records
Global complexity (variations in markets, labeling, and regulatory expectations)
Rising demand for safe AI in regulated content operations
We build a controlled, modern content foundation—then layer automation and AI where it’s safe, qualified, and valuable.
We’re a hands-on team of architects, platform leads, analysts, and go-to-market specialists who combine deep ECM engineering with Life Sciences delivery discipline. We don’t just “implement tools”—we modernise regulated content operations across Documentum, Veeva Vault, and Salesforce Life Sciences Cloud with a focus on governance, validation-readiness, and measurable adoption.
What our team believes
Compliance-first, value-driven: build control and auditability first—then automate safely.
Integration is the strategy: connect content to business processes so users don’t fight the platform.
Change sticks when adoption is designed: UX, training, and operating models matter as much as technology.
“Modernisation without disruption.”
I design migration and integration blueprints that move regulated content safely—preserving metadata, audit trails, and business continuity. My focus is connecting Documentum/Veeva content to enterprise workflows and platforms (including Salesforce LSC), with validated, low-risk delivery.
“Turn regulated requirements into working outcomes.”
I map Regulatory/Quality/Clinical needs into clear user journeys, process definitions, and data/metadata models—so the platform matches how teams actually work. My role is ensuring governance, approvals, and compliance controls are practical and adopted.
“Make the platform reliable, secure, and scalable.”
I lead the engineering that keeps ECM running at enterprise scale—upgrades, performance, security hardening, and automation. I translate complex Documentum/Veeva requirements into stable solutions that teams can operate confidently in regulated environments.
“Make our value clear to the market.”
I turn our delivery capability into clear, buyer-friendly messaging—focused on Life Sciences outcomes: inspection readiness, content control, faster retrieval, and lower cost of ownership. I also shape the story for miDocs and our platform-led approach.