The ‘Good Distribution Practice for Medical Device in Singapore’ is a regulatory framework initiated by SAC (Singapore Accreditation Council) to support the Health Products Act 2007 by HSA (Health Science Authority).
GDPMDS is a mandatory audit for any organizations involved with importing, wholesale and distribution of medical devices prior to their license application.
How will I benefit?
- Help your organization to regulate each stage of the distribution chain of medical devices
- Fulfill the requirements of GDPMDS throughout your trading process from manufacturer to wholesaler to industry and private customer
Who should attend?
- Quality managers within an organization seeking or maintaining registration to GDPMDS
- Decision makers on management system strategy
- Design Engineers, Process Engineers and Manufacturing Engineers
- Internal Auditors
- Management Team
What will I learn?
- Knowledge of medical devices fundamentals
- GDPMDS requirements audit experience sharing
- How to prepare an execute an internal audit
- How to do corrective and follow up actions to improve GDPMDS efforts
What is included?
- Delegate workbook
- Lunch and refreshments (Applicable for classroom only)
- On completion, you'll be awarded an internationally recognized BSI Training Academy certificate
