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