Brims Updates
- Mon-Fri - 8:00am - 18:00pm
- 0800 600 216 (Toll Free)
Adverse events following immunisation (AEFI) which is also vaccine safety surveillance was handed over to BoMRA from the Expanded Programme of Immunisation (EPI) in March 2021. This was followed by a series of engagements with DHMTs and the revitalisation of the National AEFI Committee. This is a committee of experts within the medical field who offers independent scientific advice to BoMRA and EPI on vaccine safety issues.
Download AEFI Forms
Looking to do some work offline, download the Adverse Events following Immunization (AEFI) forms.
The Medicines Regulatory Authority (“Authority”) is a corporate body, established under Section 3 of the Medicines and Related Substances Act (“MRSA”) and referred to as the Botswana Medicines Regulatory Authority or BoMRA. The Authority is responsible for ensuring the safety, efficacy, and quality of medicines and related substances, which includes both human and veterinary medicines, medical devices, and cosmetics in Botswana.
Designed And Developed By Ntebogang Technologies
Covid19 Updates