عرض 13–24 من أصل 33 نتيجة

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      Qualification and Validation, Documentation, Data Logging, and Data Integrity, QMS and Control

      SAR  6,900
      قراءة المزيد
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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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      Advanced Course in Bioequivalence: In-Depth BE Study Requirements for SFDA Compliance

      SAR  4,260
      قراءة المزيد
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      Qualified Person form Pharmacovigilance (QPPV)

      SAR  3,277
      قراءة المزيد
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      Common Technical Document (CTD) for Registration of Human Drugs Online Training Course

      SAR  1,380
      قراءة المزيد
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      Qualified Person form Pharmacovigilance (QPPV)

      SAR  3,277
      قراءة المزيد
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      Qualified Person form Pharmacovigilance (QPPV)

      SAR  3,277
      قراءة المزيد
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      Advanced Module 3 Content for Biologics & Biosimilars

      SAR  6,200
      قراءة المزيد
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      Advance Pharmacovigilance: Signal Detection, PV Audit & Inspection

      SAR  4,485
      قراءة المزيد
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      Validation, Verification and Transfer of Analytical Procedures

      SAR  1,719
      Date

      1.5.2024

      Location

      Online

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      Regulatory Compliance on Biosimilar & Biological

      SAR  3,900
      Date

      5.5.2024

      Location

      Online

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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

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