26 Jan Guideline For Electronic Submission of Clinical Trial Documents (Amendments, Bioequivalence Studies, Responses, Notifications, And Serious Adverse Events)
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This guideline serves as a guide to applicants on the electronic submission process for major activities performed within Clinical Trials Unit (CTU).
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Download archived version (DO NOT USE)
Download archived version (DO NOT USE)
Document Number:
SAHPGL-CEM-CT-01
Version:
3
Date Updated:
05/09/2022
File Type:
pdf
Category:
Guideline