عرض 13–22 من أصل 22 نتيجة

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    TECHNICAL REQUIREMENTS FOR CTD MODULE 3 (3.2.S/3.2.P)

    SAR  4,200
    Date

    29.4.2024
    Location

    Riyadh – Saudi Arabia
    قراءة المزيد
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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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    Essential of Drug Regulatory Affairs CTD

    SAR  3,450
    Date

    22 October 2023
    Location

    Online
    قراءة المزيد
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    BIOEQUIVILANCE IN TECH TRANSFER PRODUCTS

    SAR  2,062
    Date

    20 & 21 September 2023
    Location

    Amman, Jordan
    قراءة المزيد
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    Pharmacovigilance for QPPV

    SAR  4,370
    Date

    18 May 2023
    Location

    Online
    قراءة المزيد
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    Advanced Regulatory Affairs Training – focus on CMC/Quality Part

    SAR  4,800
    Date

    1 & 2 March 2023
    Location

    Riyadh – Saudi Arabia
    قراءة المزيد
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    Impurities and Degradation in Drug Products

    SAR  4,800
    Date

    15 – 16 March 2023
    Location

    Riyadh – Saudi Arabia
    قراءة المزيد
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    Qualified Person for Pharmacovigilance QPPV

    SAR  3,800
    Date

    26 September 2021
    Location

    Online
    قراءة المزيد
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    Technical File for Saudi Regulation for Medical Devices

    SAR  3,000
    Date

    30 June 18-20 May, 2021
    Location

    Online
    قراءة المزيد
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    New Approach of Process Validation

    SAR  5,520
    Date

    19 & 20 July 2023
    Location

    Jeddah – Saudi Arabia
    قراءة المزيد
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