When you’re manufacturing medical devices, sweeping changes in the industry, rising prices and regulatory demands are challenges you need to meet with the help of an experienced and trusted partner. SGS’s services help you adapt to rapidly changing business environments whilst giving your products reliability, resilience and distinction.
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We provide audits against recognized certification schemes that cover quality management systems in the EU, the U.S. and around the world. Whether you’re manufacturing in-vitro devices or thermometers, our assessments are robust and transparent, offering you not just an assurance of safety and efficacy, but a competitive edge that comes from demonstrating regulatory trust.
With global resources you’ll be able to access our industry specialists. They’ll give you a fresh pair of eyes, guiding your product to market more quickly whilst demonstrating best practice and improved risk management.
EU Medical Devices Regulations Information Center
Access important documents to guide your MDR and IVDR certification applications in our information center.