Basic info
Industry
medical equipment manufacturing
Sectors
Post Market Surveillance activities
Logistics
Clinical Evaluation Plan
Center of Disease Control
medical supplies
Sourcing
Consulting
MEDDEV Compliance
Digital Assets Management
Medical Device
Supply Chain Management
Systematic Literature Reviews
Risk Management
Class II & III Medical Device
FDA
Health Canada
PPE
ISO 14971:2012 Compliance
Purchasing
Clinical Evaluation Reports
Risk Benefit Analysis
Quality Management System
Gap Assessments
GDPR Compliance
Doc Control
PMA
Sourcing & Logistics
Calculating Risk
Notified Body
Procurement
MDR/MDV Filing
Pharmaceutical Drug Safety and Vigilance
Literature Reviews
Supplier Quality
Patient Safety Assessments
Medical Input
Risk Assessments
Corrective Action Preventive Actions
Performance Evaluation Plan
Recalls
CDC
Health Hazard Evaluations
Field Corrective Action
Severity of Harm estimation
Performance Evaluation Reports
In Vitro Diagnostic Devices
BSI
Food & Drug Administration
Complaint Handling
Medical Devices
Probability of Occurrence of Harm (P2) Estimation
CAPA
510k
Sales
Date founded
2017