The Product Stewardship Advantage

The medical device industry is facing a new wave of regulatory expectations, with increased scrutiny on chemical safety, material transparency, and lifecycle responsibility. As global standards evolve, manufacturers must demonstrate more than just product performance; they should also show clear accountability for how materials are selected, managed, and evaluated for sustainability. This shift presents notable challenges, including limited visibility into material composition, complex chemical regulations, and a growing need for structured toxicology and risk assessment practices.

This whitepaper offers a clear view of these industry shifts and what they mean for manufacturers. It provides practical guidance for organizations seeking to enhance their Product Stewardship approach, highlighting ways to integrate greater visibility, compliance readiness, and sustainability into the product lifecycle. By outlining the core elements of a modern stewardship framework, companies can advance safer, more compliant, and environmentally responsible products without slowing innovation.

Key learnings from this whitepaper include:

• How shifting global chemical regulations are shaping product design, material choices, and compliance expectations.
• The importance of centralized chemical data and supplier traceability in improving visibility and reducing compliance risk.
• How toxicology insights and exposure assessment support safer, more informed material selection.
• Ways to integrate sustainability and circular economy principles into product development and lifecycle planning.
• How digital tools and regulatory intelligence enable proactive, scalable stewardship programs aligned with future requirements.