Pharmacovigilance for QPPV
Pharmacovigilance for QPPV SAR  3,277
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VALIDATION, VERIFICATION, AND TRANSFER OF ANALYTICAL METHODS
VALIDATION, VERIFICATION, AND TRANSFER OF ANALYTICAL METHODS SAR  4,485
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Common Technical Document and Electronic Common Technical Document (CTD/eCTD) Online Workshop

SAR  1,380

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Qualified Person form Pharmacovigilance (QPPV)

SAR  3,277
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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

SAR  2,165
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Common Technical Document (CTD) for Registration Of Human Drugs

SAR  1,380
Date

27 February 2024
Location

Online
Registration Expired
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Technical File for Saudi Regulation for Medical Devices

SAR  3,000
Date

30 June 18-20 May, 2021
Location

Online
Registration Expired
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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
Registration Expired
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Impurities and Degradation in Drug Products

SAR  4,800
Date

15 – 16 March 2023
Location

Riyadh – Saudi Arabia
Registration Expired
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Validation, Verification and Transfer of Analytical Procedures

SAR  1,719
Date

1.5.2024
Location

Online
Registration Expired
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Essential of Drug Regulatory Affairs CTD

SAR  3,450
Date

22 October 2023
Location

Online
Registration Expired
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