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MDR 2017/745
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Home
QMS Support
ISO Management System
Trainings – ISO & Regulatory Affairs (Medical & Pharmaceuticals)
MDSAP – Medical Device Single Audit Program
Usability & HFE
VMP IQ/OQ/PQ Validation
Regulatory Support
MDR 2017/745
Medical Devices EU Compliance & Regulatory Support
EU Design Approval Support
Medical Devices Registration to South America
CE MARK
EU Auth. Rep.
UKCA
Contact US
