The South African Health Products Regulatory Authority (SAHPRA) invites industry stakeholders to attend a webinar on the launch of new modules within the SAHPRA Portal.
This webinar will provide an overview of newly introduced portal functionalities designed to enhance regulatory processes, improve data quality, and support digital transformation initiatives. Stakeholders will receive guidance on the purpose, requirements, and use of the new modules, as well as an opportunity to engage directly with SAHPRA on implementation expectations.
Date: 26 August 2026
Time: 13:00 – 15:00
Discussion Areas
- Medicines Registration Database (ISO IDMP Data Collection)
- Health Products Master Register – (ISO IDMP Data Collection) Introduction to ISO Identification of Medicinal Products (IDMP) data requirements.
- Process to link products on Health Products Master Register to existing products on applicant profile
- Process to update missing ISO IDMP data fields for linked products
- Applications for Submission of Advertising and Marketing Materials
- Licensing holders: Enrolment and Legacy data process
- New applications process for SAHPRA Licenses
- Traceability implementation – Step 1
- Logging batch details for locally manufactured batches
- Logging batch details for proposed imported batches
- New applications process for Import Authorisations for all scheduled products imported into South Africa
We look forward to your participation!
