Basic info
Industry
medical equipment manufacturing
Sectors
Medical Device
EUAR
FDA
ISO 13485
21 CFR Part 820
PMA
Responsible Person
Regulatory
Clinical Trials
Risk Management
510K
Quality Management System
UKRP
UKCA
Regulatory Approvals
Consulting
IVDR
Consultancy
CE Marking
MDR
Design Control and Design History Files
IVDs
Date founded
2008