Data Consulting for Pharmaceutical & Biotech
Your batch records live in one system, your trial data in another, and your TGA submissions get assembled by hand.
GxP-compliant data layers, consolidated clinical trial reporting, and automated regulatory submissions – without ripping out your LIMS.
The Challenges
Problems we solve every day.
Batch tracking and GxP compliance data is scattered across systems
Your LIMS holds lab results. SAP holds production records. Quality management has the deviation logs. When an auditor asks for the full batch history, someone spends two days pulling it together from five different sources.
Learn more →Multi-site clinical trial data isn’t consolidated
Each trial site submits data in a slightly different format. Your biostatistics team spends more time cleaning and reconciling than analysing. Protocol deviations get caught late because nobody has a single view.
Learn more →Regulatory submissions are assembled manually every time
TGA submissions, stability reports, and pharmacovigilance data get copy-pasted from spreadsheets into templates. Your regulatory affairs team is too senior to spend their days on data assembly – but they do.
Learn more →Integration
The systems we connect for pharmaceutical & biotech.
How We Work
Three steps to a data foundation that works.
The Data Blueprint
AI-Powered DiagnosticMaps every system, quantifies every gap, and delivers a costed roadmap with ROI already proven.
The Data Foundation
Your Single Source of TruthClean data, connected systems, and the priority capabilities that run on top — dashboards, automated reporting, and AI.
Data Command Centre
Monitor. Evolve. Scale.Ongoing management, monitoring, and evolution of your data infrastructure as your business grows.
Proof
Audit-ready compliance infrastructure for regulated substance tracking
Automated
compliance reporting
Days → minutes
audit preparation time
Full
chain of custody traceability
For a regulated healthcare provider, we built audit-ready data infrastructure for controlled substance tracking – the same compliance-first approach we bring to pharma. Automated reporting replaced manual assembly, and every record is traceable from source to submission.
A regulated healthcare provider
Insights
Related reading.
Ready to sort your pharma data out?
No sales pitch. No 90-slide deck. A direct conversation with the people who'll actually do the work.