Medical Device Vigilance Course

Medical Device & Classification

Global Medical Device Regulations

Fundamentals Of Medical Devices & Regulatory Warning Letters

Fundamentals of Medical Devices, Software in medical devices & Device Labelling

Regulatory pathways- 510(k) and PMS

Medical Device Post Market surveillance and Complaint Handling

Medical Device Post Market surveillance and Complaint Handling (Complaint vs Feedback vs Non-complaint)

mdv test

Medical Device Post Market surveillance and Complaint Handling (Complaint vs Feedback vs Non-complaint)

Complaint Intake/ triage process and practical scenarios

Complaint Evaluation Process and practical Examples.

Complaint Handling Global Decision tree process and initial report submission

Different regulatory reporting, Complaint Investigation, follow-up/final reporting and close complaints

Investigation related examples, follow-up/final reporting/close complaints and QA