We are proud to announce the release of our latest white paper
Sustainability in Medical Devices – Implications for Manufacturers and Regulators
In June 2025, confinis published a white paper on sustainability in the medical device industry, highlighting the urgent need to reduce carbon emissions while maintaining patient safety and regulatory compliance.
The healthcare industry contributes to 5% of global carbon emissions, with single-use medical devices accounting for approximately 80% of this footprint. Despite this, sustainability adoption in MedTech has been slow due to regulatory constraints prioritizing safety over environmental considerations.
This white paper explores how medical device companies can integrate sustainability across the product lifecycle, from design and development to manufacturing, packaging, and disposal, while anticipating evolving regulations and international standards. It provides practical insights and compliance-oriented strategies for sustainability leaders, product developers, and regulatory professionals.
What’s Inside
If you are working with medical devices and aiming to integrate sustainability into your strategy, this white paper is essential reading. It breaks down the environmental impact across the device lifecycle and provides clear insights into design, manufacturing, packaging, and disposal. Whether you are addressing single-use device challenges, exploring reprocessing options, or aligning with evolving international standards, you’ll find actionable guidance to strengthen your compliance strategy while reducing your environmental footprint.
Download the White Paper
Download now and take the first step toward building a sustainable medical device strategy that meets future regulatory expectations!”
Partner with confinis
At confinis, we provide expert guidance to help medical device manufacturers navigate the evolving regulatory landscape. Get in touch with us today to ensure compliance and innovation go hand in hand.
