COVID-19 Updates
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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 Botswana Medicines Regulatory Authority (BoMRA) Was established through the Medicines and Related Substances Act of 2013. The MRSA Authorises BoMRA to perform functions given by the shareholder – The Government of Botswana. The MRSA of 2013 replaced the repealed Drugs and Related Substances Act No.
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 Covid19 Updates