ISO 13485: 2016, MDSAP, FDA, 93/42/EEC Medical devices Consulting - ISO Consulting - ISO 9001, ISO 14001, ISO 45001, CE, RoHS, Reach Consulting and 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 - Introduction of the consulting process, Registration procedure of Quotation for Training and Consulting Services according to ISO 13485: 2016 I. General introduction to consulting services and benefits from consultancy of Quality Management System (QMS) according t <Detail>

ISO 13485 with Medical Device Single Audit Program (MDSAP) and 93/42/EEC Medical devices Consultant

ISO 13485 with Medical Device Single Audit Program (MDSAP) and 93/42/EEC Medical devices Consultancy The Medical Device Single Audit Program allows an MDSAP recognized Auditing Organization to conduct a single regulatory audit of a medical device manufacturer that satisfies the relevant requirement <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 with Medical Device Single Audit Program (MDSAP) and 93/42/EEC Medical devices Consultant

ISO 13485 with Medical Device Single Audit Program (MDSAP) and 93/42/EEC Medical devices Consultant

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