ISO 13485: 2016, MDSAP, FDA, 93/42/EEC Medical devices Consulting - ISO Consulting - ISO 9001, ISO 14001. ISO 45001, IATF 16949. CE, RoHS, Reach Consulting, Certification in Vietnam

ISO 13485: 2016 Consultancy - Quality management system in the field of manufacturing and providing medical devices. Introduction of the consulting process, Registration procedure of Quotation for Training and Consulting Services ISO 13485: 2016

ISO 13485:2016 CONSULTANCY & CERTIFICATION SUPPORT SERVICES Medical Devices Quality Management System (MDQMS) Introduction to the Consulting Process and Registration Procedure for ISO 13485:2016 Training, Consulting and Certification Support Services I. Introduction to ISO 13485:2016 Consultin <Detail>

ISO 13485:2016 WITH MEDICAL DEVICE SINGLE AUDIT PROGRAM (MDSAP) AND EU MEDICAL DEVICE REGULATION (MDR) CONSULTANCY

Training, Consulting and Certification Support Services for Medical Device Manufacturers Accessing Global Markets I. Introduction The global medical device industry is increasingly regulated by stringent quality management, safety, performance and regulatory requirements. Manufacturers seeking acc <Detail>

VINTECOM International delivers MDR training and technical file consulting under Regulation (EU) 2017/745 for Merap Group toward CE Marking for the EU market.

Training & Consulting Program on CE Marking Product Technical File under Regulation (EU) 2017/745 (MDR) As regulations governing medical devices in Europe become increasingly stringent, full compliance with the legal requirements of the European Union has become a prerequisite for Vietnamese pro <Detail>

ISO 13485: 2016 Consultancy - Quality management system in the field of manufacturing and providing medical devices. Introduction of the consulting process, Registration procedure of Quotation for Training and Consulting Services ISO 13485: 2016

ISO 13485: 2016 Consultancy - Quality management system in the field of manufacturing and providing medical devices. Introduction of the consulting process, Registration procedure of Quotation for Training and Consulting Services ISO 13485: 2016

ISO 13485:2016 WITH MEDICAL DEVICE SINGLE AUDIT PROGRAM (MDSAP) AND EU MEDICAL DEVICE REGULATION (MDR) CONSULTANCY

ISO 13485:2016 WITH MEDICAL DEVICE SINGLE AUDIT PROGRAM (MDSAP) AND EU MEDICAL DEVICE REGULATION (MDR) CONSULTANCY

VINTECOM International delivers MDR training and technical file consulting under Regulation (EU) 2017/745 for Merap Group toward CE Marking for the EU market.

VINTECOM International delivers MDR training and technical file consulting under Regulation (EU) 2017/745 for Merap Group toward CE Marking for the EU market.

Please choose our services :

Our clients