Basic info
Industry
medical equipment manufacturing
Sectors
Pharmaceutical
Usability Testing
ISO 13485 Quality Management Systems
FDA Registration
ISO 14971 Risk Management
Internal and Supplier Audits
Custom Quality System Development
CE Marking
Health Care
QMS Training
Regulatory Strategy
EU Authorized Representative
Audit Preparation
Clinical Studies
European Technical Files
Design Controls
Design File Remediation
510(k) Submissions
Medical Device
Medical
Contract Design
Risk Management
Mock FDA Inspection
Date founded
1999