Good Distribution Practice for Medical Devices Training Course

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.

Who should attend?

  • Quality managers or implementers 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 
  • Implementation of GDPMDS in medical device manufacturing firms
  • How to prepare an execute an internal audit
  • How to do corrective and follow up actions to improve GDPMDS efforts

What are the benefits?

  • Help your organization to regulate each stage of the distribution chain of medical devices
  • Implement and fulfill the requirements of GDPMDS throughout your trading process from manufacturer to wholesaler to industry and private customer

What is included?

  • Training course notes
  • Lunch
  • Refreshment
  • Certificate of attendance