Build digital capabilitythat lasts
For cell & gene therapy, pharma, water-quality, and aerospace organisations that need validated systems. Built embedded with your team, then handed over.
Seasoned practitioners
who deliver the work
When you engage DCC, the practitioner who scopes the work is the one who delivers it. Our team brings direct, hands-on experience: managing GxP infrastructure in cleanroom environments, validating LIMS and QMS systems under 21 CFR Part 11, and shaping IT roadmaps for GxP facilities end to end.
We build and validate systems, then transfer the capability to run them. After an engagement, your team owns the competency.
We document, train, hand over and/or maintain. Your team should be able to work, extend, and govern the systems we built. A successful engagement ends with DCC being unnecessary or in a role your organisation feels comfortable with.
What we deliver
Regulated application development
Production-grade applications for GMP environments — from environmental monitoring dashboards to quality management workflows. Built on scalable architectures that satisfy both IT governance and validation requirements.
Compliance architecture
Designing compliance into digital infrastructure from the ground up. We map regulatory requirements to technical controls during design.
GxP infrastructure management
Running the IT and OT infrastructure that underpins regulated production — qualified networks, validated server estates, identity controls, and the host platforms beneath your EMS, BMS, LIMS, and QMS. We manage change control, qualification status, and periodic review.
Capability transfer
Your team runs the systems after we leave. We embed with your people, co-develop solutions, and conduct structured knowledge transfer, so your people own the result.
IT roadmapping for regulated sites
Technology roadmaps that account for validation timelines, GMP change control, and phased deployment in live production environments. From maturity assessment through execution planning.
System integration
Connecting EMS, BMS, LIMS, QMS, and ERP into a single digital platform. We handle data extraction, environmental monitoring integration, and quality management system connections for regulated manufacturing.
Selected references
Applied in cell & gene therapy, pharma, water-quality testing, aerospace, energy and academic publishing.
The people who do the work
Train on an ATMP Q/LIMS
before go-live
NextCell is a working ATMP training environment at our Leiden office: a Simploud Q/LIMS configured for ATMP workflows, with simulated EMS/BMS, equipment and operator interfaces. Teams practise GMP processes (batch records, environmental monitoring, deviation handling, equipment qualification) on it before go-live.
Built around a unified Q/LIMS environment, powered with our partner Simploud · Hosted in Leiden, NL
Let's discuss your situation
Or email info@dccompany.org — we respond within one business day.
Based in Leiden; clients in the Netherlands, the EU and the US.
Rijnsburgerweg 10, 2333 AA Leiden