Master Data Management (MDM) for Life Sciences
Standardize, unify and govern life sciences data to drive regulatory compliance, accelerate clinical trials, enhance supply chain visibility and optimize commercial operations.
Simplify Complex Life Sciences Data Management
Achieve your most challenging business goals — from compliance reporting and interoperability to clinical trial management — with Profisee MDM.
Adverse event reporting
Maintain data integrity across the enterprise for accurate and complete adverse event reporting for regulatory bodies like ICH, FDA and EMA
Clinical trial management
Integrate, deduplicate and cleanse trial participant data from patient records, investigator sites and third-party research organizations (CROs)
HCO & HCP segmentation
Accurately segment and target healthcare organizations (HCOs) and healthcare providers (HCPs) to engage effectively while maintaining compliance
Interoperability across systems
Create seamless data flows across R&D, manufacturing, regulatory and commercial systems to fuel AI, analytics and compliance at scale
Product lifecycle tracking
Build a single source of truth for product data, automate complex workflows and stay on top of data quality and stewardship requirements
Personalize patient care plans
Deliver targeted therapies and precise genomic medicine initiatives for better patient engagement and medical outcomes
Life Sciences Master Data Management Use Cases
Clinical Trial Recruiting
“How can we integrate trial participant data from third-party sources to improve recruiting for global studies?”
How Profisee Helps
Consolidate participant data across systems to eliminate duplicates, standardize records and deliver trusted data for better recruiting and compliance.
Compliance & Adverse Event Reporting
“How can we ensure data integrity across systems for accurate compliance reporting?”
How Profisee Helps
Create trusted, duplicate-free records by unifying adverse event data across systems to support reliable reporting and analytics.
HCP & HCO Segmentation
“How can we ensure we’re targeting the right surgeons for our medical devices?”
How Profisee Helps
Unify and cleanse HCP data to ensure accurate contact, location and specialty details — supporting precise targeting and territory planning.
Personalized Medicine
“How can we access integrated patient data across EHRs to support personalized medicine?”
How Profisee Helps
Match and unify patient records across EHRs to create complete health profiles that enable safer, more precise and effective care.
Product 360
“How can we centralize BOM and raw material tracking to reduce errors and improve compliance?”
How Profisee Helps
Unify product data across systems to track components accurately, reduce manufacturing errors and support compliant operations.
Resources for Life Sciences Companies
Life Sciences Frequently Asked Questions
How can master data management improve regulatory compliance in life sciences?
MDM ensures that regulatory reporting data — such as master data and related metadata about adverse event reports, clinical trial submissions and product lifecycle documentation — is clean, complete and auditable. By creating a single source of truth, life sciences companies can streamline compliance with regulatory bodies like FDA, EMA and ICH, reducing reporting errors and audit risks.
How does MDM enhance clinical trial efficiency?
Clinical trials require integrating and managing large volumes of patient, investigator and site data from multiple sources. MDM eliminates duplicate records, standardizes data formats and ensures accurate participant matching. This allows research teams to recruit eligible candidates faster, improve trial data quality and maintain alignment across third-party clinical research organizations (CROs).
How can MDM optimize supply chain and manufacturing operations in life sciences?
Life sciences companies rely on complex global supply chains, often working with multiple suppliers, manufacturers and distributors. MDM unifies supplier and product data, ensuring better traceability, inventory management and regulatory compliance. By providing a centralized, accurate view of raw materials, components and finished products, MDM helps reduce supply chain disruptions, improve forecasting and enhance overall operational efficiency.
How does MDM support mergers, acquisitions and system migrations in life sciences?
Life sciences companies frequently acquire new businesses, leading to data silos across multiple CRM, EHR, ERP and regulatory systems. MDM enables rapid data consolidation and migration, ensuring that customer, patient, provider and product data is harmonized, deduplicated and ready for unified reporting. This results in a faster post-merger integration process and more reliable enterprise-wide analytics.
Discover how the Profisee platform helps build and ensure a
trusted foundation of life sciences data.
