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

منتجات ذات صلة

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Pharmacovigilance for QPPV

SAR  4,370
Date

18 May 2023
Location

Online
قراءة المزيد
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Pharmacovigilance for QPPV

SAR  3,277
قراءة المزيد
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Qualified Person form Pharmacovigilance (QPPV)

SAR  3,277
قراءة المزيد
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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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Qualified Person form Pharmacovigilance (QPPV)

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

SAR  3,900
Date

5.5.2024
Location

Online
قراءة المزيد
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Manufacturing Process Validation for Regulatory Affairs & Process Validation for Sterile Products

SAR  4,200
قراءة المزيد
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VALIDATION, VERIFICATION, AND TRANSFER OF ANALYTICAL METHODS

SAR  4,485
قراءة المزيد
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