SFDA workshop on quality variation in pharmaceutical products (Requirements and conditions)

<p style="direction: ltr;">» Objectives<br />
&nbsp; During this workshop all relevant aspects regarding the quality assessment of post approval changes in pharmaceuticals will be discussed. You will get to know:<br />
&nbsp; &nbsp; &nbsp; -&nbsp; Understanding the requirements of minor and major variations.<br />
&nbsp; &nbsp; &nbsp; -&nbsp; Learn about some commonly encountered deficiencies and how to address them.<br />
&nbsp; &nbsp; &nbsp; -&nbsp; The current guidance and risk assessment for nitrosamine impurities.</p>

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<p style="direction: ltr;">&nbsp; &nbsp; &nbsp; &nbsp; <a href="https://surveys.sfda.gov.sa/zs/jqCCEO">Registration Link</a></p>