We visit with Greg Jones from SGS North America and gain insight into the ISO 13485 certification process from a seasoned auditor. Start-ups or established medical device manufacturers can benefit from this discussion as we speak about potential pitfalls that could jeopardize accreditation.
Guest Description:
Greg Jones is the Technical Director at SGS in North America. In that capacity, Greg is responsible for all technical and operational aspects of medical device certification including ISO 13485, MDSAP, MDR and IVDR. Greg brings over 15 years of experience in Medical Device Certification and prior to that spent over 10 years in Research & Development as a Process Engineer with a leading Medical Device manufacturer. He is a certified lead auditor for ISO 9001 and ISO 13485. Greg earned his Bachelors at Belmont University.
201.296.5353
Email [email protected]
We visit with Greg Jones from SGS North America and gain insight into the ISO 13485 certification process from a seasoned auditor. Start-ups or established medical device manufacturers can benefit from this discussion as we speak about potential pitfalls that could jeopardize accreditation.
Guest Description:
Greg Jones is the Technical Director at SGS in North America. In that capacity, Greg is responsible for all technical and operational aspects of medical device certification including ISO 13485, MDSAP, MDR and IVDR. Greg brings over 15 years of experience in Medical Device Certification and prior to that spent over 10 years in Research & Development as a Process Engineer with a leading Medical Device manufacturer. He is a certified lead auditor for ISO 9001 and ISO 13485. Greg earned his Bachelors at Belmont University.
201.296.5353
Email [email protected]