Basic info
Industry
medical equipment manufacturing
Sectors
UKMDR
21CFR
Clinical Evaluation
Quality Assurance
Surveillance
Supplier Controls
Regulatory
Medical Devices Bill 2019-21
Regulatory as a Service
ISO 13485
Quality
ISO 14971
RaaS
QMS
Compliance
Medical Device
MHRA
Grace Period
MDR
Post Market
CAPA
Risk Management
Date founded
2020