Join SGS at Booth 534 during The MedTech Conference, October 15-17, 2024, in Toronto, ON. We’ll be highlighting our expertise in helping medical device companies meet global regulatory requirements while ensuring product safety and consistent quality.
Visit us to explore:
- Regulatory Compliance: Learn how SGS supports your journey through the EU MDR/IVDR regulatory landscape, ensuring smooth conformity assessments for your medical devices.
- Certification & Compliance: We offer medical device CE marking as a Notified Body through our affiliate in Belgium (1639) and in Finland (0598) for Software as a Medical Device (SaMD) certification. SGS is also a UK Approved Body (0120) for conformity assessments under the UKCA scheme and an Auditing Organization (AO) for MDSAP certification.
- Tailored Testing Solutions: Explore our comprehensive testing services, including microbiological, chemical, and product quality testing, to ensure your devices meet international standards.
Don’t miss our EU MDR/IVDR Regulatory Update - Panel Session on Wednesday, October 16, from 10:45–11:45 AM (Room 715), featuring SGS experts Ibim Tariah and Balazs Bozsik. This session will provide practical insights into navigating EU regulatory challenges, the conformity assessment process, and potential improvements for manufacturers.
At SGS, we provide full-solution support to help medical devices reach the market safely and efficiently. With a global network of more than 2,700 offices and laboratories, SGS ensures your products meet the highest regulatory and quality standards. Visit Booth 534 to learn how we can help you succeed in the evolving medtech industry.
For further information, please contact:
Dominic James
Marketing Assistant
t: +1-862-339-6737
201 Route 17 North,
7th and 8th Floors,
Bloomfield, New Jersey, 07003,
United States