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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