SGS Medical Devices

Next week, we will be at the 32nd International Precision Med TRI-CON in San Diego, California! From March 11-13, you can find us at booth 8. Team members Supreeya Sansawat - VP, Food, Life Sciences at SGS, Balazs and Daniel Fisher will be available to answer all of your questions about medical device certification, audit and training. We can help you to reach new markets and ensure regulatory compliance for your devices. Learn more: https://bit.ly/4aYadpK #MedicalDevices #MedicalDeviceCertification #SGSNorthAmerica

We're thrilled to be attending two exciting Regulatory Affairs Professionals Society (RAPS) events next month in Baltimore, Maryland! The Global Regulatory Strategy Conference, March 11-12, provides insights into top trends and upcoming regulatory challenges. The Regulatory Intelligence Conference, March 13-14, aims to provide a deep dive into regulatory intelligence and policy best practices. Both events bring together medical device and pharmaceutical regulatory affairs professionals. Visit table 10 during these conferences to meet with SGS experts Gregory Jacobson and Ibim Tariah. We look forward to meeting you! Global Regulatory Strategy Conference: https://bit.ly/4gD6WgN Regulatory Intelligence Conference: https://bit.ly/4hIqIZG #MedicalDevices #MedicalDeviceCertification #SGSNorthAmerica

Enroll in one of our upcoming virtual Medical Device Regulation (MDR) training courses and save 20%! This is a limited time offer applicable to March course dates. MDR Clinical Evaluation equips learners with the knowledge and skills needed to navigate the complexities of clinical investigation and post-market surveillance. USA, use code MDR3USA20 https://bit.ly/41kV3b2 CAN, use code MDR3CA20 https://bit.ly/41k9Y5k MDR Post Market Surveillance provides in-depth insights into the regulatory landscape governing post-market surveillance activities, as well as the tools needed to navigate Annex III compliance. USA, use code MDR5USA20 https://bit.ly/40XV7vW CAN, use code MDR5CA20 https://bit.ly/4b4PQqU #MedicalDevices #MDR #MDD #SGSNorthAmerica

The medical device team had an amazing time last?week at MD&M Trade Shows West in Anaheim! We had the opportunity to connect with some of our clients and other industry experts on the latest innovations and regulations in the medical device industry. Thanks again to all who stopped by our booth! #MedicalDevices #MedicalDeviceCertification #SGSNorthAmerica

We are proud Gold Sponsors for the Regulatory Affairs Professionals Society (RAPS) San Francisco Chapter 2025 Kick Off meeting! Our team will be in San Francisco on January 12 for the event. Stop by the SGS booth to speak with Balazs Bozsik, Technical Director - Medical Devices, and Daniel Fisher, Regional Sales Manager - Medical Devices. Register here ?? https://bit.ly/40nPsAn #MedicalDevices #MedicalDeviceCertification #SGSNorthAmerica

We are proud to be Gold Sponsors for this event! Join us on January 12 for the RAPS San Francisco Bay Area Chapter 2025 Kick-Off Meeting. Balazs Bozsik and Daniel Fisher will be at the SGS Booth. #MedicalDevices #MedicalDeviceCertification #SGSNorthAmerica

Cyber Week is here – all SGS Academy public training courses are 30% off! ??? This time of year is perfect for staying ahead of ever-changing industry standards, gaining a competitive edge and investing in your professional growth for less. Sign up for expert-led training courses on quality, sustainability or social responsibility. ?? Book your training now: USA: https://bit.ly/4cIzHH1 CAN: https://bit.ly/4ek8Pyr Promo codes THANKSUSA30 (USA) and THANKSCA30 (Canada) are valid from Dec 2 - Dec 6 on any courses scheduled through March 31, 2025. #SGSAcademy #Training #SGSNorthAmerica

The medical device team is in Orlando, FL this week for BioFlorida, Inc. Florida Innovation Conference! We're here to discuss your medical device certification, audit and training needs. Stop by Booth # 11 with any questions you might have about MDR, ISO 13485, MDSAP, UKCA, or overall regulatory compliance. Gregory Jacobson and Daniel Torres are happy to help! #MedicalDevices #MedicalDeviceCertification #SGSNorthAmerica

As the EU MDR has raised the level of scrutiny required to place a device on the EU market, startup cardiovascular device manufacturers must have a good understanding of how to make the EU Regulatory process work for them. In a recent webinar, Ibim Tariah and Gregory Jacobson discussed the requirements for regulatory compliance in the areas of device classification, conformity assessment, GSPRs, CE marking, post market surveillance, and more. Now available on demand: https://bit.ly/3Ust4Cd #MedicalDevices #MDR #MDD #Cardiovascular #CardiovascularDevices #EURegulations #SGSNorthAmerica

SGS is a proud Bronze Sponsor for next week's MPO Summit in Denver, Colorado! Ibim Tariah, Gregory Jacobson, Tim Ryan, and Tim Gooch are attending this networking and educational event for medical device manufacturers. Tim Gooch will be presenting "Extending Your Global Reach and Minimizing Your Compliance Exposure at Home" on Thursday October 31 from 11:30 - 12:15pm. This session will cover MDSAP and the US FDA's adoption of ISO 13485, the recognized framework for design and manufacturing compliance for medical device. Learn more about Tim's speaking session ?? https://bit.ly/401wjnY #MedicalDevices #ISO13485 #MDSAP #SGSNorthAmerica