Completing the Quality/ CMC Module of the CTD & Impurities Interactive Workshop
Completing the Quality/ CMC Module of the CTD & Impurities Interactive Workshop SAR  4,600
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Medical Device Regulation – Regulatory Frameworks & SFDA Updates
Medical Device Regulation – Regulatory Frameworks & SFDA Updates SAR  2,300
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QPPV Training Feb 2026
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QPPV Training

SAR  3,277

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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)

SAR  3,277
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Qualified Person form Pharmacovigilance (QPPV)

SAR  3,277
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Qualified Person form Pharmacovigilance (QPPV) Online Training

SAR  3,277
قراءة المزيد
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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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Regulatory Compliance on Biosimilar & Biological

SAR  3,900
Date

5.5.2024
Location

Online
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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
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