Bayer: Customer Data Strategies for Reduction in Costs and Complexity

Veeva Systems Inc

@VeevaSystems

Published: July 26, 2019

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This video provides an executive perspective from Bayer on their successful customer data strategy, centering on the implementation of a Veeva solution and the strategic utilization of Veeva Open Data to achieve substantial reductions in operational costs and complexity. The speaker immediately quantifies the financial impact of this transition, noting that the initial shift to the Veeva platform resulted in an immediate savings of half a million dollars. This initial success established a strong business case for further investment in data centralization and optimization.

The core strategy involved getting rid of disparate reference data sources and extending the use of Veeva Open Data across multiple critical commercial and regulatory functions. Key operational areas benefiting from this integration include state license validation, which is crucial for ensuring field representatives can legally engage with healthcare professionals, and managing sample ability, which governs compliant distribution of drug samples. By centralizing this reference data, Bayer significantly streamlined these processes, reducing the manual effort and complexity historically associated with maintaining accurate, up-to-date compliance data.

Furthermore, the company leveraged the Veeva Open Data platform for transparency reporting, a mandatory and data-intensive regulatory requirement tracking payments and interactions with healthcare providers. This expansion generated additional, ongoing savings by simplifying the data aggregation and reporting process. Critically, the savings realized from reducing data complexity and eliminating reliance on expensive, external reference data providers are not being retained as simple cost cuts but are being strategically channeled back into the program. These funds are earmarked for future innovation, specifically supporting projects related to data science and broader digital enablement initiatives, demonstrating a self-funding model for advanced commercial capabilities.

The long-term vision involves further integration of the centralized data asset across the enterprise. The speaker mentions plans to extend the use of Open Data to the Medical CRM system, indicating a move toward unifying data governance and ensuring consistency between commercial and medical affairs activities. This strategic reinvestment into data science and digital platforms highlights how foundational data management improvements are essential prerequisites for successful AI and advanced analytics initiatives within the highly regulated pharmaceutical environment.

Key Takeaways:

  • Quantifiable ROI on Platform Migration: The initial transition to the Veeva solution delivered an immediate and significant return on investment, with Bayer achieving $500,000 in savings, validating the financial benefits of modernizing core commercial data infrastructure.
  • Veeva Open Data as a Cost Reduction Engine: Strategic adoption of Open Data allowed Bayer to eliminate reliance on costly, complex third-party reference data services, directly reducing vendor spend and the internal overhead associated with data harmonization and maintenance.
  • Compliance Automation for Field Operations: The centralized data platform is instrumental in automating critical regulatory checks, specifically state license validation and sample eligibility, ensuring continuous compliance for sales representatives and reducing risk associated with non-compliant interactions.
  • Streamlining Regulatory Transparency: Extending the use of Open Data to transparency reporting simplifies one of the most data-intensive regulatory requirements in the pharmaceutical industry, yielding further operational savings and enhancing the accuracy of required disclosures.
  • Self-Funding Innovation Model: The cost savings achieved through data optimization are strategically reinvested into high-value initiatives, including data science and digital enablement, creating a sustainable financial model for continuous technological advancement.
  • Foundation for Data Science: By standardizing and cleaning customer reference data, the company establishes a high-quality data foundation, which is a prerequisite for successful deployment of AI and machine learning models in commercial operations.
  • Integration with Medical Affairs: Future plans to integrate Open Data into the Medical CRM system signal a strategic effort to unify data governance between commercial and medical teams, crucial for compliant and coordinated engagement with healthcare professionals (HCPs).
  • Focus on Complexity Reduction: Beyond monetary savings, the primary benefit is the reduction in complexity across data technology and service providers, which improves data quality, reduces IT burden, and accelerates time-to-insight for commercial teams.

Tools/Resources Mentioned:

  • Veeva Solution: Refers generally to the suite of Veeva products utilized by the pharmaceutical industry, likely including Veeva CRM and related data services.
  • Veeva Open Data: A specific Veeva product providing verified, standardized healthcare professional (HCP) and healthcare organization (HCO) reference data, which is central to the cost-saving strategy.
  • Medical CRM: The Customer Relationship Management system used by Medical Affairs teams, indicating a planned integration point for the centralized data.

Key Concepts:

  • Reference Data: The foundational, standardized data (like HCP names, addresses, specialties, and affiliations) required for commercial operations, compliance, and reporting. Managing this data efficiently is critical for pharma companies.
  • State License Validation: The mandatory process of verifying that healthcare professionals hold current, valid licenses in the states where they practice, a key compliance requirement for pharmaceutical interactions.
  • Sample Ability: The process of determining a healthcare professional's eligibility to receive drug samples, which is strictly governed by FDA regulations and state laws.
  • Transparency Reporting: Regulatory reporting (e.g., U.S. Sunshine Act, European equivalents) that requires pharmaceutical companies to disclose payments and transfers of value made to healthcare professionals and organizations.

Examples/Case Studies:

  • Bayer's Initial Savings: The company achieved an immediate savings of half a million dollars simply by shifting their reference data management to the Veeva solution.
  • Strategic Reinvestment: The savings generated are being explicitly redirected to fund new projects in data science and digital enablement, demonstrating a commitment to leveraging operational efficiency gains for future innovation.