SFDA accomplish writing a couple of guidelines

<p>SFDA has accomplished some of its guidelines in contribution with a specialized committees includes experts and drug liables at Saudi levels; those guidelines are based on the higher and up to dates quality standers in drug monitoring and regulations worldwide.</p>
<ul>
<li>Institutions and Pharmaceutical Products Guidelines.</li>
<li>Institutions and Pharmaceutical Products Guideline Regulations. </li>
<li>Narcotic Guidelines</li>
<li>Narcotic Regulations</li>
<li>Drugs Companies and Its Products Registration Guideline.</li>
<li>Herbal Products &amp; Food Supplements Companies Registration Guideline.</li>
<li>Radiopharmaceuticals </li>
<li>Manufacturing and Compounding of Medications in Pharmacies and Hospitals Guidelines</li>
<li>Good Manufacturing Practice (GMP) Guidelines </li>
<li> Post-Marketing Surveillance (PMS) Guidelines*<ul><li>The SFDA Responsibility in PMS. </li><li>PMS Guidelines for Human Drugs. </li><li> PMS Guidelines for Veterinary Drugs. </li><li>PMS Report for Human Drugs. </li><li> PMS Report for Veterinary Drugs. </li></ul></li>
<li>Good Laboratory Practice (GLP) Guidelines </li>
<li>Clinical Trials Guidelines.</li>
<li>Bioequivalence Guidelines. </li>
<li>Stability Guidelines. </li>
</ul>