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  • About us
    • Who we are
    • Board
    • Executive Management
    • Expressions of Interest
    • Quality Management System
    • Regulatory Partnerships
    • Special Projects
      • Backlog
    • Vacancies
    • Tenders
  • Operational Units
    • Biologicals
      • Communication to Industry
      • Forms
      • Guidelines
    • Complementary Meds
      • Application portal
      • Communication to Industry
      • Forms
      • Guidelines
      • Templates
    • Clinical Trials
      • Communication To Industry
      • Forms
      • Guidelines
    • Inspectorate and Regulatory Compliance
    • 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
      • Acts and Regulations
      • Forms
      • Guidelines & Codes of Practice
      • News & Updates
    • Safety Information
      • Covid-19 Adverse Events Report
      • Health Product Vigilance
      • Product Recalls
      • Rapid Alerts
      • Recalls Reporting
      • Report Side Effects
      • Safety Alerts
    • Unregistered Products
      • Category A Medicines
      • Complementary Medicines
      • Medical Devices
      • Veterinary Medicines
    • Veterinary Medicines
      • Guidelines
      • Registered Vet Products
      • Veterinary Portal
  • Databases & Registers
    • Medical Devices Licences Issued
    • OTC Medicines Directory
    • Pharma Licenced Establishments
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    • PI & PIL Repository
    • Registered Health Products
    • Registered Vet Products
  • E-Services
    • Adverse Drug Reaction Reporting
    • AEFI Reporting Dashboard
    • Complementary Medicines Licensing
    • COVI-VIG Reporting System
    • Health Product Application Status Checker
    • Lot Release Search
    • OTC Medicines Directory
    • Product Variations Portal
    • Med Safety App
    • Registered Health Products
    • Section 21 Applications
    • Variations Status Checker
    • Veterinary portal
  • E-Library
    • Corporate & Publications
      • Annual Reports
      • Documents For Comments
      • Fees
      • Newsletters
      • Planning Documents
      • Position Statements
      • Published Papers
    • Forms
    • Guidelines
      • Guidelines Notice Board
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Regulatory Partnerships

International Pharmaceutical Regulators Programme (IPRP)

WHO – Prequalification of Medicines Programme

International Council for Harmonisation (ICH)

African Vaccine Regulatory Forum (AVAREF)

African Medicine Regulatory Harmonisation (AMRH)

International Clinical Trials Registry Platform

European Medicines Agency

International Medical Device Regulators Forum

International Narcotics Control Board

Pharmaceutical Inspection Co-operation Scheme

WHO Uppsala Monitoring Centre

VICH

CONTACT US

General Enquiries
For general, non-product specific enquiries only.
enquiries@sahpra.org.za

For Emergencies
For emergencies only.
emergency@sahpra.org.za

 

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