Medical devices and pharmaceuticals require detailed, structured data—including specifications, formulations, classifications (GTIN, UDI, GUDID), and multilingual packaging details. But managing this information across disconnected systems leads to errors, inconsistencies, and compliance risks.
Pharmaceuticals and medical devices require highly regulated digital assets—including IFUs (Instructions for Use), safety data sheets, 3D models, certification documents, and marketing materials. Without a centralized DAM system, version control, localization, and regulatory approvals become chaotic.
Compliance with FDA (U.S.), MDR (EU), UDI (Unique Device Identification), ISO standards, and GxP regulations requires accurate, up-to-date product documentation. Managing certifications, safety reports, and audit trails across global markets is time-consuming and error-prone.
Pharmaceutical and medical device companies operate in heavily regulated international markets. Managing multi-language product catalogs, country-specific compliance documents, and localized labeling at scale is complex without automation.
Ensuring consistent product data across eCommerce, distributor networks, regulatory portals, and supply chain systems is critical. But manual updates, disconnected platforms, and lack of real-time synchronization cause delays and inconsistencies.
Many manufacturers rely on outdated, fragmented IT systems to manage product data, compliance documents, and digital assets. Maintaining multiple disconnected platforms increases operational costs, slows down innovation, and creates bottlenecks in regulatory approvals.
The healthcare and life sciences industry depends on precise data management, regulatory compliance, and seamless digital asset distribution to support medical device manufacturers, pharmaceutical companies, and biotech firms. Yet, many businesses struggle with fragmented product information, disconnected regulatory workflows, and inconsistent digital experiences—leading to inefficiencies, compliance risks, and slower time-to-market.
This is where Product Experience Management (PXM) transforms the industry. PXM unifies data and experience management, enabling companies to centralize product information, manage compliance documents, streamline digital asset distribution, and automate multi-channel content syndication—all from a single platform.
Healthcare and life sciences companies face challenges such as inconsistent product specifications across regulatory submissions, delays due to manual documentation workflows, and difficulties in managing global labeling and compliance requirements. Pimcore’s PXM solution integrates Product Information Management (PIM), Master Data Management (MDM), Digital Asset Management (DAM), Customer Data Platform (CDP), Digital Experience Platform (DXP), and Digital Commerce to ensure data accuracy, regulatory efficiency, and seamless global distribution.
PXM isn’t just a tool—it’s the key to accelerating compliance, optimizing product data, and driving scalable growth in healthcare and life sciences.
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