The MedTech industry is evolving rapidly, with advancements in medical devices, in vitro diagnostics and digital health solutions transforming patient care. However, companies face increasing regulatory requirements, complex supply chains and stringent safety standards.
We help you navigate these challenges with comprehensive testing, inspection, certification and regulatory compliance services. From product development and production to market entry and post-market surveillance, our global expertise supports your MedTech innovation at every stage.
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Discover the benefits of our MedTech services
- Ensure regulatory compliance and market accessOur regulatory services help you meet global medical device regulations, from FDA, EU MDR and IVDR compliance to ISO 13485 certification, ensuring your products meet the highest safety and performance standards.
- Enhance patient safety and product qualityThrough rigorous testing, risk assessments and performance evaluations, we help you verify device safety, reliability and effectiveness.
- Streamline product development and approvalWe provide expert guidance, clinical evaluation support and regulatory strategy insights to reduce the time-to-market while maintaining compliance.
- Improve supply chain transparency and securityOur auditing, traceability and supplier verification services help mitigate risks and strengthen the integrity of your MedTech supply chain.
Global expertise and trusted solutions for the MedTech industry
As the world’s leading testing, inspection and certification company, we provide specialized MedTech solutions to help manufacturers, suppliers and distributors ensure product quality and compliance.
Our global network of experts, state-of-the-art laboratories and regulatory knowledge enable us to support your journey from innovation to market success.
Partnering with us means working with a trusted leader dedicated to ensuring the safety and effectiveness of medical technologies.
