Industries

Pharmaceutical

Accelerate discovery-to-launch with compliant, data-driven operations. From R&D data platforms and trial execution to manufacturing quality and pharmacovigilance—we help you move faster without compromising safety or integrity.

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R&D Data Foundations
ELN/LIMS interoperability • FAIR data • Lineage & traceability
Trial Execution
eConsent • ePRO/COA • Risk-based monitoring & query management
Manufacturing & Quality
GMP controls • Batch records • Deviation/CAPA & release workflows
Who we serve

Focus Areas

From early discovery and clinical development to tech ops and medical affairs—each card shows where we unlock value first.

Discovery & Preclinical

  • Assay data pipelines & ontology mapping
  • ELN integrations, results review & signoff
  • IP protection, access controls & audit trails

Clinical Development

  • Study build, randomization & visit schedules
  • RBQM dashboards, queries & reconciliation
  • Data cleaning, locks & submission readiness

Manufacturing & Supply

  • MES/eBR, weigh & dispense, genealogy
  • Release testing, stability & cold-chain views
  • Deviations, CAPA & change control

Pharmacovigilance & Medical

  • Case intake, triage & signal detection
  • Aggregate reports & benefit–risk
  • Scientific exchange & content approvals
What we deliver

Solution Programs

Choose a track or combine them for end-to-end transformation. Every program includes governance, controls, and measurable outcomes.

R&D Data Platform

  • FAIR-aligned lakehouse & catalogs
  • Terminology services & mappings (CDISC/MedDRA)
  • Secure workspaces for analytics & modeling

Trial Acceleration

  • Study build automation, eCOA & monitoring
  • Data reconciliation & automatic queries
  • Submission packaging & document control

Quality & Compliance Ops

  • GxP validation, traceability & release gates
  • Deviation/CAPA workflows & trending
  • Audit trails, evidence packs & SLOs
Why it matters

Outcomes We Target

-22–37%Time from LPLV to database lock
+13–21%Site activation velocity
99.977%+GxP platform uptime SLO
-28–44%Deviation/CAPA cycle time
How we work

Validated Delivery, Accelerated

  1. 1

    Discover

    Process maps, risks & controls, SLAs/SLOs, data & validation needs.

  2. 2

    Design

    Target architecture, data/standards strategy, migration waves & test plans.

  3. 3

    Build

    Secure SDLC, validation packages, automation, performance & resilience checks.

  4. 4

    Operate

    SRE practices, monitoring, audits, inspection readiness & continuous improvement.

Ecosystem

Standards, Platforms & Tools

GxP21 CFR Part 11ICH E6/E8 CDISC (SDTM/ADaM)MedDRAIDMP HL7 FHIRDICOMOpenID/OAuthSAML PostgreSQLKafkaRedis KubernetesTerraformVault/KMS PrometheusGrafanaOpenTelemetry SnowflakeBigQuerydbt

Advance molecules to medicines—safely and at speed.

We’ll align opportunities, risks, and a pragmatic roadmap your teams can execute—within the quality, privacy, and reliability standards regulators and patients expect.

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