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Scrip Regulatory Affairs
Tanzania identifies 16 device categories to kick-start first phase of registration drive
24 November 2009
Vibha Sharma

The Tanzanian Food and Drugs Authority is asking manufacturers of 16 categories of medical devices to formally register their products with the agency as part of its efforts to establish a medtech regulatory framework for the country1.

The first phase of the registration process is set to commence on 1 January 2010 and it will last for 24 months, ie until 31 December 2011...

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