Course Content
-
Day One: SS620:2016 – Good Distribution for Medical Devices-Requirements
- Scope
- Normative References
- Terms and Definitions
- Quality Management System
- Management Responsibility
- Resource Management
- Premises and Facilities
- Secondary Assembly
- Traceability
- Counterfeit, Adulterated, Unwholesome or Tampered Medical Devices
- Complaint Handling
- Field Safety Corrective Action (FSCA)
- Internal Audit
- Outsourced Activities
- Class-room Exercise & Discussion
-
Day Two: ISO 19011:2018 Guidelines for Auditing
- Part 1: Auditing Requirements
- Part 2: Auditing Exercise
Prev
Scope