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

      SAR  6,900
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      Intellectual Property, Patents and Regulatory Affairs: Key Drivers in the Pharmaceutical Industry Strategy

      SAR  3,910
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      Strategic Components for Tech. Transfer in Pharmaceutical industry

      SAR  4,370
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      Advanced Course in Bioequivalence: In-Depth BE Study Requirements for SFDA Compliance

      SAR  4,260
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      Qualified Person form Pharmacovigilance (QPPV) Online Training

      SAR  3,277
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      Qualified Person form Pharmacovigilance (QPPV)

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

      SAR  1,380
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      Qualified Person form Pharmacovigilance (QPPV)

      SAR  3,277
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      Qualified Person form Pharmacovigilance (QPPV)

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

      SAR  6,200
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