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Trusted Reporting &Operational
Intelligence

Across multiple engagements, Peraison partnered with Elekta, a publicly listed global medical equipment provider, to improve the accuracy and reliability of reporting and monitoring across finance, compliance, and service operations.

 

Finance reporting was automated and governed to support IFRS, US GAAP, SEC disclosure expectations, and SASB Medical Equipment and Supplies standards, replacing spreadsheet-led workflows and reducing inconsistent regional numbers.

 

In compliance, we consolidated device logs and alerts, generated device-level compliance KPIs, detected early indicators of failure, and produced mandated regulatory PDF reports aligned to frameworks including EU MDR, US FDA expectations, ISO 13485, and MDSAP audits.

 

In operations, we enabled insight-driven monitoring of maintenance cycles and machine alerts, including automated ticketing and device profiling, to reduce downtime risk across global client sites.

 

Peraison continues to host and operate the analytics environment as an extension of Elekta’s teams, keeping reporting governed, consistent, and always available as business needs evolve.

Customer Story
Public company-grade reporting accuracy and audit defensibility

Improved consistency of reported numbers across regions by replacing manual spreadsheet assembly with governed definitions and automated reporting workflows, reducing audit and compliance exposure.

Compliance reporting shifted from weeks of manual effort to automated intelligence

Automated regulatory reporting and compliance monitoring reduced manual effort to near zero, improved traceability, and surfaced early warning indicators so issues could be addressed before they threatened compliance.

Reduced downtime risk and faster operational response

Strengthened maintenance control and accelerated response to machine alerts through automated monitoring and ticketing, improving operational reliability across global service teams.

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Modern Data Solutions for 
pharmaceuticals & Biotech

Accelerating Pharma & Biotech With Data & AI

  • Bring together research and laboratory data with scientific knowledge to prioritise targets and make faster go or no-go decisions. Enable teams to compare results across studies, reduce duplication, and collaborate with confidence, cutting time spent reconciling inputs and accelerating progression from discovery to development.

  • Improve trial feasibility, site selection, enrolment, and delivery by combining operational data from start-up, monitoring, and site performance. Link clinical, patient-reported, imaging, and real-world data to strengthen evidence, shorten timelines from first patient in to database lock, and improve decision-making.

  • Use patient, investigator, and site data to improve recruitment, retention, and diversity outcomes. Identify drop-off points, optimise outreach and communications, and prioritise sites that deliver. Provide clear performance views that help clinical teams intervene early and keep studies on track across regions.

  • Strengthen data governance, traceability, and audit readiness across GxP processes with controlled datasets and clear lineage. Improve inspection readiness, reduce remediation effort, and support submission-ready reporting by embedding quality checks, validation-aligned controls, and consistent definitions across clinical, safety, quality, and manufacturing data.

  • Accelerate case processing and strengthen safety monitoring with better data quality, automation, and analytics across pharmacovigilance workflows. Integrate safety, clinical, and medical data to support faster triage, earlier detection of emerging issues, and more consistent reporting, while reducing manual effort and operational backlog

  • Improve batch visibility, quality performance, and supply reliability by connecting CMC, manufacturing, and logistics data end to end. Identify drivers of deviations, yield loss, and downtime, strengthen release readiness, and support planning decisions that protect service levels and reduce cost across sites and partners.

  • Build modern data foundations that make life sciences data trusted, governed, and ready for scale. Accelerate cloud and platform modernisation, improve data quality and lineage, and enable reusable data products that support analytics, automation, and AI use cases across R&D, clinical, safety, quality, and manufacturing.

Our Pharmaceuticals & Biotech stories & insights

Explore the real‑world impact of our work across pharmaceuticals and biotech, with stories and insights showing how data, AI, and technology deliver measurable outcomes.

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Clinical Trial Onboarding Accelerator

AI-enabled clinical trial onboarding cut CG Oncology’s patient reviews from hours to minutes, automating document ingestion and eligibility assessment to scale trials without added headcount.

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Unified Finance & Supply Chain Forecasting

Unified SAP and supply-chain analytics into a single source of truth for Aspen Pharmacare Europe, accelerating close 65% and improving forecasts 40–55% significantly.

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Commercial Master
Data Management

Business-led commercial master data standardised AbbVie’s product and account reporting, improving comparability and speed through exception-led stewardship that sustains accuracy and prevents drift.

Read More
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Orthopaedics Production and OTIF Intelligence

Real-time production and OTIF dashboards gave Zimmer Biomet hourly visibility, pinpointed bottlenecks, reduced downtime, and enabled faster root-cause actions to protect deliveries reliability.

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Multi-Banner Pharmacy
Performance

Unified performance reporting across 40+ multi-banner pharmacies, combining operational and financial KPIs to cut write-offs, lift services revenue, productivity, rebates, network-wide insight.

Curious how we can improve your business's performance?

Get in touch with our team

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