Good Distribution Practice for Medical Devices is a mandatory requirement by the Health Science Authority (HSA) for any organizations involved with the handling, storage, delivery, installation, servicing, secondary assembly, and other related activities (e.g. warehousing, logistics, and freight forwarding services) of medical devices including in-vitro diagnostic devices.
Objective:
Who should attend:
Management, Quality Managers/ Executives, Internal auditors & implementers of SS 620:2016
Course Structure:
✓ Introduction to SS 620:2016 GDPMDS requirements
✓ Administration of Good Distribution Practices within the organization
✓ Fulfill HSA requirements throughout the distribution supply chains
✓ Preparation and conduct an internal audit
✓ Furnishing of the audit report and follow-up
✓ Corrective action & Improvement
Course Details:
(Note: A discount of 10% awaits if you signed up for more than 3 participants)
*Inclusive of Summarized Notes & Certificate of Attendance
For more information: