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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
  • Case Study

ULTRUS® WERCS Studio helps Bostik transform SDS authoring and compliance at global scale

See how Bostik unified SDS systems, accelerated compliance and improved efficiency across 50 countries with UL Solutions.

Bostik

Managing safety data sheets (SDS) at global scale can quickly become complex, especially when systems are fragmented and regulatory demands continuously evolve. Bostik, a global leader in adhesives, faced these challenges head-on as it expanded into new markets and industries.

By partnering with UL Solutions and deploying WERCS Studio, Bostik replaced five disconnected tools with a single, centralized platform for SDS authoring, regulatory screening and global distribution.

The transformation enabled seamless integration with Enterprise Resource Planning (ERP) and other enterprise systems, automated SDS distribution workflows and improved data consistency across operations. With built-in regulatory intelligence powered by ChemADVISOR®, Bostik can rapidly respond to changing requirements and maintain compliance across 50 countries and 47 languages.

This modernized approach delivered measurable impact — reducing manual effort, improving reporting accuracy and accelerating critical regulatory processes, including cutting Poison Centre Notification (PCN) submission times by at least 60%.

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