Qualified Person form Pharmacovigilance (QPPV) SAR  3,277
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Manufacturing Process Validation for Regulatory Affairs & Process Validation for Sterile Products SAR  4,200
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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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Qualified Person for Pharmacovigilance QPPV

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26 September 2021

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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

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

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Validation, Verification and Transfer of Analytical Procedures

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Date

1.5.2024

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Common Technical Document (CTD) for Registration Of Human Drugs

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27 February 2024

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Pharmacovigilance for QPPV

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Date

18 May 2023

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Impurities and Degradation in Drug Products

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15 – 16 March 2023

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