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

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Date

27 February 2024
Location

Online

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BIOEQUIVILANCE IN TECH TRANSFER PRODUCTS

SAR  2,062
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20 & 21 September 2023
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18 May 2023
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19 & 20 July 2023
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Site Inspection Preparation & Readiness

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Regulatory Compliance on Biosimilar & Biological

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Quality Management Systems – Risk Management – Risk Assessment and Control

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Qualified Person form Pharmacovigilance (QPPV)

SAR  3,277
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