The Challenge

A global biopharma found it difficult to manage patient data across multiple systems and geographies. Different therapy areas had their own ways of storing and validating patient information, which made it complex to track patient journeys, consent versions and engagement activities across the markets they operated in. 

Key Challenges included:

  • Fragmented Patient Data
    Patient data was not uniform. Each market had a different CRM or portal, which meant that one patient could exist as multiple records in different systems. The lack of a single identity created issues when commercial and digital teams wanted to engage them in a unified manner. 
  • Consent and Privacy Concerns
    Each country had its own compliance rules for patient consent (GDPR, HIPAA). However, the teams didn’t have a real-time system to validate if consent was up to date or valid at the time of use. This created operational slowdowns and audit risk. 
  • Data Duplication and Inconsistency
    When affiliates shared patient data, the same record was being duplicated and stored in separate repositories. This duplication caused inconsistencies in analytics and downstream activation. 
  • No Master Identifier
    There was no unique ID that connected a patient across systems. This made it difficult to know which touchpoints belonged to which patient, and it delayed insights generation on engagement outcomes. 
  • Disconnected Systems
    CRM, SAP, and analytics systems were not integrated. Any reconciliation was manual and time consuming. 

Our Solution

Agilisium designed and implemented a centralized Patient Identity Management (IDM) framework that unified patient records, consent data, and system-level integrations into one connected backbone. 

1
Democratized Data Access
Developed a non-SQL method for querying data within the EDF, eliminating the need for SQL knowledge.

Identity Resolution Engine

An engine was built using Azure Data Factory and Databricks that matched records across systems using deterministic and probabilistic logic. This created a golden patient record and reduced duplication drastically. 

2

Consent Lifecycle Management

We introduced a digital consent registry integrated with CRM tools like Salesforce and Veeva. This allowed the compliance teams to validate and track patient consent in real time across regions.

3

Data Governance and Stewardship

A governance layer was added to maintain audit readiness. The lineage of every patient record was tracked from source to usage, with role-based access to data stewards and compliance users.

4

FHIR-based Interoperability

APIs were deployed to standardize data flow between different systems, allowing updates and consent changes to sync automatically.

5

Secure Cloud Framework

The entire setup was hosted on Azure with encryption and masking standards using Purview and Key Vault to meet all privacy regulations.

Key Impact
98%
Accuracy achieved in patient matching and de-duplication.
70%
Reduction in manual reconciliation work across systems.
The Customer
The customer is a leading global biopharmaceutical company that works across oncology, cardiovascular and immunology therapy areas

The Outcomes

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Unified View. Continuous Compliance.

The patient IDM framework connected all patient data into one backbone. Now, commercial, compliance and digital teams work off the same repository when they engage patients or review consent history. 

One Record, One Source

The golden record acts as the master version for every patient across systems, giving consistent information across therapy and region. 

Faster Consent Validation

The digital consent registry automatically validates every consent version before activation, making it easier to stay compliant without delay. 

Interoperable Data Exchange

FHIR-based APIs allow seamless integration between CRM, patient portals, and analytics systems.

Analytics Enablement

The data is now ready for patient engagement dashboards that show activation, adherence and journey-level insights.

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