Basic info
Industry
medical equipment manufacturing
Sectors
CE - marking
Clinical Evaluation
IEC 62304
Software
IVDR
IEC 62366-1
Regulatory
MDD
FDA and QSR
Consulting
ISO 13485
Quality
STED
Training
Due Diligence
European-authorized-representative
ISO 14971
Medical Device regulations
UK Responsible Person
MDR
Performance Evaluation
IVDD
Risk Management
Date founded
2013