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        Common Technical Document (CTD) for Registration of Human Drugs Online Training Course

        SAR  1,380
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        Common Technical Document and Electronic Common Technical Document (CTD/eCTD) Online Workshop

        SAR  1,380
        Registration Expired
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        Completing the Quality/ CMC Module of the CTD & Impurities Interactive Workshop

        SAR  4,600
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        Completing the Quality/ CMC Module of the CTD & Impurities Interactive Workshop – 16 & 17 June 2026

        SAR  4,600
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        CTD and eCTD training course

        SAR  1,380
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        Essential of Drug Regulatory Affairs CTD

        SAR  3,450
        Date

        22 October 2023
        Location

        Online
        Registration Expired
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        ICH E6(R3) Training Program Under the auspices of Mesned Pharma Consult Center In Cooperation with ICH Experts from Egyptian Drug Authority

        SAR  2,165
        Registration Expired
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        Impurities and Degradation in Drug Products

        SAR  4,800
        Date

        15 – 16 March 2023
        Location

        Riyadh – Saudi Arabia
        Registration Expired
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        Intellectual Property, Patents and Regulatory Affairs: Key Drivers in the Pharmaceutical Industry Strategy

        SAR  3,910
        Registration Expired
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        Manufacturing Process Validation for Regulatory Affairs & Process Validation for Sterile Products

        SAR  4,200
        Registration Expired
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        Medical Device QMS

        Medical Device Quality Management Systems (QMS)

        SAR  4,140
        Registration Expired
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        Medical Device Regulation – Regulatory Frameworks & SFDA Updates

        SAR  2,300
        Registration Expired
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