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About us
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Executive Management
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eCTD Submissions Portal
Quality Management System
Regulatory Partnerships
Agreements/MOUs
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Forms
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Inspectorate and Regulatory Compliance
Importation – Border Control
Medical Devices
Communication to Industry
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Guidelines
Conformity assessment bodies
Licenced Establishments
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Related Documents
Test Kits
Names and Scheduling
Amended Schedules
Consolidated Schedules
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Orthodox Medicines
Communication to Industry
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Registered Health Products
Templates
Radiation Control
Communication To Industry
Acts and Regulations
Forms
Templates
Guidelines & Codes of Practice
Inspection bodies
News & Updates
Safety Information
Pharmacovigilance
Covid-19 Adverse Events Report
Health Product Vigilance
Product Recalls
Rapid Alerts
Recalls Reporting
Report Side Effects
Safety Alerts
Unregistered Products/Section 21
Category A Medicines
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– Updated 07 November 2024
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