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About us
Who we are
Board
Executive Management
Expressions of Interest
Digital Transformation
eCTD Submissions Portal
Quality Management System
Regulatory Partnerships
Agreements/MOUs
Special Projects
Backlog
Vacancies
Tenders
Operational Units
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Communication to Industry
Forms
Guidelines
Complementary Meds
Application portal
Communication to Industry
Forms
Guidelines
Templates
Clinical Trials
Communication To Industry
FAQs
Forms
Guidelines
Inspectorate and Regulatory Compliance
Importation – Border Control
Medical Devices
Communication to Industry
Forms
Guidelines
Conformity assessment bodies
Licenced Establishments
Position Statements
Related Documents
Test Kits
Names and Scheduling
Amended Schedules
Consolidated Schedules
Guidelines
Orthodox Medicines
Communication to Industry
Forms
Guidelines
Registered Health Products
Templates
Radiation Control
Communication To Industry
Acts and Regulations
Forms
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
Complementary Medicines
Medical Devices
Veterinary Medicines
Veterinary Medicines
Guidelines
Registered Vet Products
Veterinary Portal
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Medical Devices Licences Issued
OTC Medicines Directory
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PI & PIL Repository
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E-Services
Adverse Drug Reaction Reporting
AEFI Reporting Dashboard
Complementary Medicines Licensing
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eCTD Submissions Portal
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Active Pharma Licenced Establishments
Version 33
– Updated 10 June 2024
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