National Drug Authority hosted a stakeholders’ consultative workshop on medical devices on 29^th September 2009. The aim of the workshop was to discuss proposals for strengthening of regulation of medical devices in Uganda contained in the following drafts documents: (1) guideline for registration of medical devices, and (2) guideline for registration of malaria RDTs

Click  the links below to see a detailed reports

1. The draft documents 
2.  Workshop report.

 Comments may be sent to ndaug@nda.or.ug