Regulatory Affairs (CTD/eCTD) Workshop - SFDA Requirements
Regulatory Affairs (CTD/eCTD) Workshop - SFDA Requirements SAR  1,380
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Biosimilar Regulatory Submission Training
Regulatory Submission of Biosimilars with a Focus on Chinese Portfolios SAR  4,150
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Training for Scientific Office Manager Online training

SAR  4,000

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

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

SAR  4,200
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29.4.2024
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Riyadh – Saudi Arabia
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Advanced Course in Bioequivalence: In-Depth BE Study Requirements for SFDA Compliance

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Advance Pharmacovigilance: Signal Detection, PV Audit & Inspection

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Pharmacovigilance for QPPV

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18 May 2023
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Pharmacovigilance for QPPV

SAR  3,277
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Common Technical Document (CTD) for Registration Of Human Drugs

SAR  1,380
Date

27 February 2024
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Qualified Person form Pharmacovigilance (QPPV)

SAR  3,277
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