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