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13 July 2017
Workshop between the Regulator and Industry on Medical Devices

Following the promulgation of the Medicines and Related Substances Amendment Act (2015), Act 14 of 2015, the Department of Health intends to host a workshop on transitional arrangements for medical devices.

The workshop will address issues pertaining to the Roadmap for the Regulation of Medical Devices, Section 21 Authorisation, QMS requirements, Licensing and Vigilance.

Click here to download the invitation.