Essential of Drug Regulatory Affairs CTD
Essential of Drug Regulatory Affairs CTD SAR  3,450
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TECHNICAL REQUIREMENTS FOR CTD MODULE 3 (3.2.S/3.2.P)
TECHNICAL REQUIREMENTS FOR CTD MODULE 3 (3.2.S/3.2.P) SAR  4,200
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Common Technical Document (CTD) for Registration Of Human Drugs

SAR  1,380

Registeration Expired

التصنيف:
معلومات إضافية
Date

27 February 2024
Location

Online
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منتجات ذات صلة

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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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Qualified Person for Pharmacovigilance QPPV

SAR  3,800
Date

26 September 2021
Location

Online
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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
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Pharmacovigilance for QPPV

SAR  3,277
قراءة المزيد
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Quality Management Systems – Risk Management – Risk Assessment and Control

SAR  1,150
قراءة المزيد
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Technical File for Saudi Regulation for Medical Devices

SAR  3,000
Date

30 June 18-20 May, 2021
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
قراءة المزيد
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VALIDATION, VERIFICATION, AND TRANSFER OF ANALYTICAL METHODS

SAR  4,485
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