عرض 13–24 من أصل 53 نتيجة

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    Common Technical Document (CTD) for Registration Of Human Drugs

    SAR  1,380
    Date

    27 February 2024
    Location

    Online
    قراءة المزيد
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    CTD/eCTD Online Training

    Common Technical Document and Electronic Common Technical Document (CTD/eCTD)

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

    SAR  1,380
    قراءة المزيد
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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
    قراءة المزيد
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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
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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
    قراءة المزيد
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    Impurities and Degradation in Drug Products

    SAR  4,800
    Date

    15 – 16 March 2023
    Location

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

    SAR  3,910
    قراءة المزيد
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    Manufacturing Process Validation for Regulatory Affairs & Process Validation for Sterile Products

    SAR  4,200
    قراءة المزيد
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    Medical Device QMS

    Medical Device Quality Management Systems (QMS)

    SAR  4,140
    قراءة المزيد
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