The SAHPRA E-services serve as the digital gateway to streamline and facilitate regulatory processes within SAHPRA.
Offering secure and user-friendly online platforms, E-Services provides individuals and organisations with efficient access to a range of electronic services. From online applications to submissions and enquiries, users can navigate through categorised sections, ensuring a seamless experience.
Here you can report adverse drug reactions from medicines, vaccines, herbal products, biological medicines and product quality issues. Please fill in the information as complete as possible.
This portal provides information on reports of Adverse Events Following Immunisation (AEFIs) associated with COVID-19 vaccine administration.
This portal is dedicated to the provision of, and support for, the regulatory framework for Category D Medicines by SAHPRA.
This section assists patients/healthcare profressionals regarding unregistered and off-label use of medicines for the treatment and prevention of COVID-19.
SAHPRA has implemented an application status checker. This new tool is listed under “Online Services” on the SAHPRA website.
SAHPRA has implemented a variations status checker. This new tool is listed under “Online Services” on the SAHPRA website.
This portal allows members of the public to check the confirmation of the released lot of human vaccines authorised by SAHPRA.
SAHPRA’s OTC Online Medicines’ Directory provides healthcare professionals and the consumer with a guide to all SAHPRA-registered over-the counter (OTC) medicines that are available in South Africa without a doctor’s prescription.
SAHPRA’s Information Technology (IT) Unit have put in place a HelpDesk specifically for Digital Variations Portal (DVP) support. For all DVP technical or system related issues, please email: applicationsupport@sahpra.org.za.
The Med Safety App is a mobile application developed to engage both patients and healthcare providers to report on adverse drug reactions.
Our Registered Health Products List is a comprehensive database of all the approved and authorised health products that have met our rigorous standards.
The Section 21 Submission portal (for Category A Medicines for Human Use) processes and evaluates applications from applicants (treating practitioners) for access to unregistered medication within South Africa.
The VET application status checker portal allows the user to easily track the progress of your veterinary medicine or product registration application with SAHPRA.