Medical Device
We consult within quality management, project management, product development and training related to medical device products and their processes.
Fjord Consulting offers consultation, advice, coaching as well as hands-on support and training in topics related to quality management and development of medical devices.
Contact us if you have questions regarding MDD/MDR, ISO 13485, ISO 14971, EN 62366, QSR (FDA 21 CFR Part 820), and other regulations with the medical device field.
Fjord Consulting offers consultation, advice, coaching as well as hands-on support and training in issues related to development of medical devices in accordance to Design Control. Contact us if you have questions regarding MDD/MDR, ISO 13485, ISO 14971, EN 62366, QSR (FDA 21 CFR Part 820), and other regulations with the medical device field.
Fjord Consulting compile training and workshops for your board, management team, employees as well as partners and suppliers. We perform training within relevant topics related to medical devices and quality management.
Contact us regarding training in MDD/MDR, ISO 13485, ISO 14971, EN 62366, QSR (FDA 21 CFR Part 820), and other regulations with the medical device field.
Helena Hjälmefjord
Tel +46 722 51 08 69
hhj@fjordconsulting.se
