Join SGS at Booth 3827 during the Medical Design & Manufacturing (MD&M) Conference, October 16-17, 2024, in Minneapolis, MN. Discover how our comprehensive solutions can support you in bringing your medical devices to market efficiently and safely.
Visit us to discuss:
- Regulatory Compliance & Certification: Learn about CE marking for medical devices, including Software as a Medical Device (SaMD), and our certifications under the UKCA and MDSAP schemes.
- Product Testing & Quality Assurance: Explore our full range of cGMP pharmaceutical product testing services, ensuring the highest standards in quality and patient safety.
- Supply Chain Audits & Risk Management: Find out how our auditing services can help you manage risk, ensuring compliance across your supply chain.
At SGS, we help bring medical devices to market safely and efficiently. As a full-solution provider, we ensure your products meet the highest quality and regulatory requirements. We offer medical device CE marking as a Notified Body through our affiliates in Belgium (1639) and Finland (0598) for SaMD products. SGS is also a UK Approved Body (0120) and an Auditing Organization (AO) for MDSAP certification. Our global network of more than 2,700 offices and laboratories enables us to provide training, assessment, testing, and certification services worldwide.
Join us at Booth 3827 to learn how SGS can help you meet regulatory requirements and successfully bring your medical devices to market.
For further information, please contact:
Dominic James
Marketing Assistant
t: +1-862-339-6737