TRAINING
FDA Medical Device
Premarket Notification Training

ISO 13485:2016
Basic Training

ISO 13485:2016
Internal Auditor and Lead Auditor Training

ISO 14971
Risk Management Training

TRAINING
Sterilization Methods and Validation Training

CE
CE Marking:2017/745 MDR Training

TRAINING
Clinical Evaluation Training

TRAINING
Custom Need Training

SERVICES
CERTIFICATION
ISO 13485 Medical devices
Quality management systems
Requirements for regulatory purposes