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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منتجات ذات صلة

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Impurities and Degradation in Drug Products

SAR  4,800
Date

15 – 16 March 2023
Location

Riyadh – Saudi Arabia
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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
قراءة المزيد
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Validation, Verification and Transfer of Analytical Procedures

SAR  1,719
Date

1.5.2024
Location

Online
قراءة المزيد
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Essential of Drug Regulatory Affairs CTD

SAR  3,450
Date

22 October 2023
Location

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

SAR  4,200
Date

29.4.2024
Location

Riyadh – Saudi Arabia
قراءة المزيد
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Site Inspection Preparation & Readiness

SAR  1,380
قراءة المزيد
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New Approach of Process Validation

SAR  5,520
Date

19 & 20 July 2023
Location

Jeddah – Saudi Arabia
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Qualified Person form Pharmacovigilance (QPPV)

SAR  3,277
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