The Medical Device Interim Regulation Launching Workshop

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 The SFDA represented by the Medical Devices Sector intends to fulfill its responsibilities with respect to regulating medical devices to ensure their safety, quality, effectiveness and their performance according to the manufacturers intended purpose. Due to the importance of keeping the private sector, informed of the SFDA medical devices Interim regulation that has been adopted by the SFDA board of directors, its implementing rules, and the SFDA provisions regarding the medical devices companies and establishments responsibilities toward the SFDA and the medical devices from importation to disposal. The SFDA is launching three workshops in Riyadh, Jeddah and Dammam.
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<h2><b><font face="Calibri">Objectives</font></b></h2>
<p>The workshops aims to introduce the following:</p>
<p>· Medical Devices Interim Regulation. </p>
<p>· Complementing implementing rules. </p>
<p>· Registration and Licensing requirements of medical devices establishments. </p>
<p>· The Authorized Representatives requirements. </p>
<p>· The importance of rules and regulations and the implementing rules that intended to be applied in Kingdom of Saudi Arabia. </p>
<p>· Answering the attendees inquiries.</p>
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<h2><b><font face="Calibri">Workshop Dates and places</font></b></h2>
<p align="justify">Riyadh 11/7/2009 ,At Riyadh Chamber of Commerce and Industry <br />Jeddah 14/7/2009 ,At Jeddah Chamber of Commerce and Industry<br />Dammam 18/7/2009 ,At Dammam Chamber of Commerce and Industry.<br /><br /><font face="Calibri"><font size="2">for Registration please </font></font></p>