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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Site Inspection Preparation & Readiness

SAR  1,380
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Qualification and Validation, Documentation, Data Logging, and Data Integrity, QMS and Control

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Qualified Person for Pharmacovigilance QPPV

SAR  3,800
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26 September 2021

Location

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TECHNICAL REQUIREMENTS FOR CTD MODULE 3 (3.2.S/3.2.P)

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29.4.2024

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Riyadh – Saudi Arabia

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Advanced Regulatory Affairs Training – focus on CMC/Quality Part

SAR  4,800
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1 & 2 March 2023

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Riyadh – Saudi Arabia

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Impurities and Degradation in Drug Products

SAR  4,800
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15 – 16 March 2023

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Quality Management Systems – Risk Management – Risk Assessment and Control

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Manufacturing Process Validation for Regulatory Affairs & Process Validation for Sterile Products

SAR  4,200
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