South Africa medical device & IVD approval process

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FDA asks COVID test makers to switch from emergency to premarket approvals

Singapore’s HSA to commence Phase I implementation of UDI labeling in November 2022

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South Africa medical device & IVD approval process

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FDA asks COVID test makers to switch from emergency to premarket approvals

Singapore’s HSA to commence Phase I implementation of UDI labeling in November 2022

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Related Service

Software as a Medical Device (SaMD): EU/US Regulatory Considerations

Scaling and Conducting Use-Related Risk Analysis (URRA)

South Africa medical device & IVD approval process

Questions? Request more information from our specialists

Related

South Africa Medical Device Regulations

South Africa Department of Health

Have questions on what Emergo can do for you?