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