Completing the Quality/ CMC Module of the CTD & Impurities Interactive Workshop
Completing the Quality/ CMC Module of the CTD & Impurities Interactive Workshop SAR  4,600
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Medical Device Regulation – Regulatory Frameworks & SFDA Updates
Medical Device Regulation – Regulatory Frameworks & SFDA Updates SAR  2,300
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QPPV Training Feb 2026
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QPPV Training

SAR  3,277

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Common Technical Document (CTD) for Registration Of Human Drugs

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27 February 2024
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Qualification and Validation, Documentation, Data Logging, and Data Integrity, QMS and Control

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SAR  4,200
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29.4.2024
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Riyadh – Saudi Arabia
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